Search result for '156 '.
Viewing records 51 to 100 of 216 hits.
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N2106155
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Name: RED TIDE UPB1 |
Price:
£11.00
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Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
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Stock type: individual line
|
Material type: seed
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Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
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Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
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N2106156
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Name: RED TIDE WOX5 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
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Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
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Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
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N2106157
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Name: RED TIDE FEZ |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
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Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
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Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
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N2106158
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Name: RED TIDE UBQ10 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
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Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
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Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
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N2106159
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Name: RED TIDE 2x35S |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
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Stock type: individual line
|
Material type: seed
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Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
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Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
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N2106160
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Name: RED TIDE RCH1 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
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Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
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Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
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N2106161
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Name: RED TIDE RCH2 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
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Stock type: individual line
|
Material type: seed
|
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Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
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Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
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N2106162
|
Name: RED TIDE KN |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col 0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on hygromycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
RED TIDE line. Cell type specific promoter expressing a H2B-2xCherry tag in the nucleus
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
N2106171
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Name: BREAK ATHB8 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
N2106172
|
Name: BREAK IAA19 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
N2106189
|
Name: BREAK UBQ10 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
N2106190
|
Name: BREAK 2x35S |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and ACTIN2prom::BirA expressing plants were transformed by dipping. Primary transformants (T1) were selected in vitro on kanamycin. For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
BREAK line. Cell type specific promoter expressing a NTF tag in the nuclear envelope for nuclei purification using the INTACT method
|
N2106192
|
Name: LINE-UP SHR |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on glufosinate (basta). For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
LINE-UP line. Cell type specific gene induction
|
N2106193
|
Name: LINE-UP EXP7 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on glufosinate (basta). For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
LINE-UP line. Cell type specific gene induction
|
N2106194
|
Name: LINE-UP FEZ |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on glufosinate (basta). For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
LINE-UP line. Cell type specific gene induction
|
N2106195
|
Name: LINE-UP UBQ10 |
Price:
£11.00
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: seed
|
|
Description Each SWELL line construct was transformed into C58 GV3101 Agrobacterium strain and selected on YEB media (5g/L beef extract; 1g/L yeast extract; 5g/L peptone; 5g/L sucrose; 15g/L bactoagar; pH 7.2) supplemented with antibiotics (Spectynomicin, Gentamycin). After two days of growth at 28°C, bacteria were collected using a single-use cell scraper, re-suspended in about 200mL of transformation buffer (10mM MgCl2; 5% sucrose; 0.25% silweet) and Col0 plants were transformed by dipping. Primary transformants (T1) were selected in vitro on glufosinate (basta). For all constructs, around 20 independent T1 lines were isolated and six representative mono-insertion lines were selected in T2. Independent lines homozygous for the transgene were selected in T3. Some of the lines were produced later during the selection process and are distributed as segregating T2s.
|
Phenotype
LINE-UP line. Cell type specific gene induction
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
Donor
- Ecole Normale Supérieure de Lyon Yvon Jaillais
- Centre National de la Recherche Scientifique (CNRS) Gregory Vert
|
Locus
|
Stock type: individual line
|
Material type: plasmid dna
|
|
Description SAND line. Cell type specific promoter expressing a 4xYFP tag in the cytoplasm. Generated through Multisite gateway cloning. Vector resistance in bacteria: Spectinomycin. Vector backbone: pB7m34GW. Bacterial strain: DH5alpha.
|
|
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