Search results for: 'protein'
- 10 imagesATM antibody [2C1] [GRP83]
ChIP, ELISA, FACS, ICC, IF, IHC-P, IP, WB
Human, Mouse, Rat, Monkey
Mouse
Monoclonal
100 μl -
- 2 images
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- 2 images
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- 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 -
- 10 images
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- 2 images
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- 6 images
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- 2 images
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- 7 images
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![Whole cell extract (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (GRP535) diluted at 1:1000.](https://www.grp-ak.de/media/catalog/product/a/t/atm-antibody-2c1_grp535_wb_6_2.jpg)
![HeLa whole cell extract and nuclear extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (GRP535) diluted at 1:500. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](https://www.grp-ak.de/media/catalog/product/a/t/atm-antibody-2c1_grp535_wb_5_2.jpg)
![ATM antibody [2C1] detects ATM protein at nucleus by immunohistochemical analysis.Sample: Paraffin-embedded human breast carcinoma.ATM stained by ATM antibody [2C1] (GRP535) diluted at 1:100.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](https://www.grp-ak.de/media/catalog/product/a/t/atm-antibody-2c1_grp535_ihc-p_1_2.jpg)
![The WB analysis of ATM antibody [2C1] was published by Lee JH and colleagues in the journal PLoS One in 2014 .](https://www.grp-ak.de/media/catalog/product/a/t/atm-antibody-2c1_grp535_wb_4_2.jpg)
![The WB analysis of ATM antibody [2C1] was published by Kongruttanachok N and colleagues in the journal Mol Cancer in 2010.PMID: 20356374](https://www.grp-ak.de/media/catalog/product/a/t/atm-antibody-2c1_grp535_wb_3_2.jpg)
![The WB analysis of ATM antibody [2C1] was published by He D and colleagues in the journal Sci Rep in 2016.PMID: 27074761](https://www.grp-ak.de/media/catalog/product/a/t/atm-antibody-2c1_grp535_wb_2_2.jpg)
![The WB analysis of ATM antibody [2C1] was published by Gibbs-Seymour I and colleagues in the journal Aging Cell in 2015.PMID: 25645366](https://www.grp-ak.de/media/catalog/product/a/t/atm-antibody-2c1_grp535_wb_1_2.jpg)
![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)
![PAX6 antibody detects PAX6 protein by immunohistochemical analysis.Samples: Paraffin-Embedded mouse retina.Green: PAX6 protein stained by PAX6 antibody (GRP589) diluted at 1:250.Red: beta Tubulin 3/ Tuj1, stained by beta Tubulin 3/ Tuj1 antibody [GT1338]](https://www.grp-ak.de/media/catalog/product/p/a/pax6-antibody_grp589_ihc-p_2_2.jpg)
