Search results for: 'Shigella sonnei form 1'
- 9 imagesPARP antibody [GRP12]
ChIP, ICC, IF, IHC-Fr, IHC-P, IP, WB
Human, Mouse, Rat
Rabbit
Polyclonal
100 μl -
- 10 imagesPARP antibody [N2C1], Internal [GRP54]
ChIP, ICC, IF, IHC-P, IP, WB
Human, Mouse, Rat
Rabbit
Polyclonal
100 μl -
- 4 images
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- 2 images
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- 2 images
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- 2 images
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- 2 images
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- 2 images
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- 2 imagesTIMP-1 Polyclonal Antibody [GRP238]
ICC, IF, IHC-P, WB
Human, Mouse, Rat, Rabbit
Rabbit
Polyclonal
100 μl -
- 2 images
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![PARP1 antibody [N2C1], Internal detects PARP1 protein at nucleus on HeLa xenograft by immunohistochemical analysis. Sample: Paraffin-embedded HeLa xenograft. PARP1 antibody [N2C1], Internal (GRP506) dilution: 1:500.](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_ihc_1_2.jpg)
![Various whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PARP1 antibody [N2C1], Internal (GRP506) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_wb_5_2.jpg)
![Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PARP antibody [N2C1], Internal (GRP506) diluted at 1:50000. The HRP-conjugated anti-rabbit IgG antibody was u](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_wb_4_2.jpg)
![Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with PARP antibody [N2C1], Internal (GRP506) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_wb_3_2.jpg)
![Untreated (–) and treated (+) HCT116 whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with PARP antibody [N2C1], Internal (GRP506) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to de](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_wb_2_2.jpg)
![Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with PARP antibody [N2C1], Internal (GRP506) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_wb_1_2.jpg)
![PARP antibody [N2C1], Internal detects PARP protein at nucleus by immunofluorescent analysis.Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: PARP stained by PARP antibody [N2C1], Internal (GRP506) diluted at 1:500.Red: phalloi](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_icc_1_2.jpg)
![PARP1 antibody [N2C1], Internal immunoprecipitates PARP1 protein in IP experiments.IP samples: HCT-116 whole cell extractA. 30 ?g HCT-116 whole cell extractB. Control with 4 ?g of preimmune Rabbit IgGC. Immunoprecipitation of PARP1 protein by 4 ?g PARP1 a](https://www.grp-ak.de/media/catalog/product/p/a/parp-antibody-n2c1-internal_grp506_ip_1_2.jpg)
