Primary Antibodies
-
-
- Histone H2A.XS139ph (phospho Ser139) antibody [GT2311] [GRP79]
ICC, IF, IHC-P, IP, WB
Human, Mouse, Rat
Mouse
Monoclonal
100 μl -
-
- Carbonic Anhydrase IX antibody [GT12] [GRP82]
FACS, ICC, IF, IHC-Fr, IHC-P, IP, WB
Human
Mouse
Monoclonal
100 μl - ATM antibody [2C1] [GRP83]
ChIP, ELISA, FACS, ICC, IF, IHC-P, IP, WB
Human, Mouse, Rat, Monkey
Mouse
Monoclonal
100 μl -
- BRCA1 antibody [17F8] - ChIP grade [GRP85]
ChIP, ELISA, ICC, IF, IHC-P, IP, WB
Human, Mouse
Mouse
Monoclonal
100 μl - BRCA1 antibody [6B4] - ChIP grade [GRP86]
ChIP, ICC, IF, IHC-P, IP, WB
Human, Mouse
Mouse
Monoclonal
100 μl
![TET1 antibody [GT1462] detects TET1 protein at nucleus on HeLa xenograft by immunohistochemical analysis. Sample: Paraffin-embedded HeLa xenograft. TET1 antibody [GT1462] (GRP530) dilution: 1:100.](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-gt1462_grp530_ihc_1_2.jpg)
![TET1 antibody [GT1462] detects TET1 protein by western blot analysis.A. 50 μg whole cell lysate/extract from 293T cells transfected with scramble siRNA B. 50 μg whole cell lysate/extract from TET1-knockdowned 293T cells6% SDS-PAGETET1 antibody [GT14](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-gt1462_grp530_wb_3_2.jpg)
![TET1 antibody [GT1462] detects TET1 protein at nucleus by immunofluorescent analysis. Sample: TET1-transfected (right) or untransfected (left) 293T cells were fixed in 4% paraformaldehyde for 15 min. Green: TET1 protein stained by TET1 antibody (GRP530](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-gt1462_grp530_if_1_2.jpg)
![NT2D1 whole cell and nuclear extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with TET1 antibody [GT1462] (GRP530) diluted at 1:500.](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-gt1462_grp530_wb_2_2.jpg)
![Immunoprecipitation of TET1 protein from NT2D1 whole cell extracts using 5 ?g of TET1 antibody [GT1462] (GRP530).Western blot analysis was performed using TET1 antibody [GT1462] (GRP530) diluted at 1:500.EasyBlot anti-Mouse IgG was used as a secondary rea](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-gt1462_grp530_ip_1_2.jpg)
![Histone H2A.XS139ph (phospho Ser139) antibody [GT2311] detects Histone H2A.XS139ph (phospho Ser139) protein at nucleus on mouse testis by immunohistochemical analysis. Sample: Paraffin-embedded mouse testis. Histone H2A.XS139ph (phospho Ser139) antibody [](https://www.grp-ak.de/media/catalog/product/h/i/histone-h2a.xs139ph-phospho-ser139-antibody-gt2311_grp531_ihc_1_2.jpg)
![Histone H2A.X (phospho S139) antibody [GT2311] detects H2AFX protein by western blot analysis.A. 30 μg NIH-3T3 whole cell lysate/extract (untreated)B. 30 μg NIH-3T3 whole cell lysate/extract (30μM cisplatin treatment for 24hr)15% SDS-PAGEHistone](https://www.grp-ak.de/media/catalog/product/h/i/histone-h2a.xs139ph-phospho-ser139-antibody-gt2311_grp531_wb_5_2.jpg)
![Histone H2A.X (phospho S139) antibody [GT2311] detects Histone H2A.X (phospho S139) [GT2311] protein by western blot analysis. Un-treated (-) and treated (+, 30 μM Cisplatin treatment for 24 hrs) PC-12 whole cell extracts (30 μg) were separated by 1](https://www.grp-ak.de/media/catalog/product/h/i/histone-h2a.xs139ph-phospho-ser139-antibody-gt2311_grp531_wb_4_2.jpg)
![Histone H2A.X (phospho S139) antibody [GT2311] detects H2AFX protein by western blot analysis.A. 30 μg HCT116 whole cell lysate/extract (untreated)B. 30 μg HCT116 whole cell lysate/extract (30 μM cisplatin treatment for 24hr)12% SDS-PAGEHistone H](https://www.grp-ak.de/media/catalog/product/h/i/histone-h2a.xs139ph-phospho-ser139-antibody-gt2311_grp531_wb_2_2.jpg)
![The WB analysis of Histone H2A.XS139ph (phospho Ser139) antibody [GT2311] was published by En J and colleagues in the journal PLoS Negl Trop Dis in 2017.PMID: 28783752](https://www.grp-ak.de/media/catalog/product/h/i/histone-h2a.xs139ph-phospho-ser139-antibody-gt2311_grp531_wb_1_2.jpg)
![p21 Cip1 antibody [GT1032] detects p21 Cip1 protein by western blot analysis.A. 30 μg HCT116 whole cell lysate/extract (untreated)B. 30 μg HCT116 whole cell lysate/extract (30 μM Cisplatin treatment for 24 hr)C. 30 μg HCT116 whole cell lysate/](https://www.grp-ak.de/media/catalog/product/p/2/p21-cip1-antibody-gt1032_grp532_wb_4_2.jpg)
![p21 Cip1 antibody [GT1032] detects p21 Cip1 protein at nucleus by immunofluorescent analysis.Sample: Mock and treated HCT116 cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: p21 Cip1 stained by p21 Cip1 antibody [GT1032] (GRP532) diluted at](https://www.grp-ak.de/media/catalog/product/p/2/p21-cip1-antibody-gt1032_grp532_icc_1_2.jpg)
![The WB analysis of p21 Cip1 antibody [GT1032] was published by Chang TC and colleagues in the journal PLoS One in 2015.PMID: 25961745](https://www.grp-ak.de/media/catalog/product/p/2/p21-cip1-antibody-gt1032_grp532_wb_3_2.jpg)
![The WB analysis of p21 Cip1 antibody [GT1032] was published by Chang TC and colleagues in the journal PLoS One in 2015.PMID: 25961745](https://www.grp-ak.de/media/catalog/product/p/2/p21-cip1-antibody-gt1032_grp532_wb_2_2.jpg)
![The WB analysis of p21 Cip1 antibody [GT1032] was published by Chang TC and colleagues in the journal PLoS One in 2015.PMID: 25961745](https://www.grp-ak.de/media/catalog/product/p/2/p21-cip1-antibody-gt1032_grp532_wb_1_2.jpg)
![p21 Cip1 antibody [GT1032] immunoprecipitates CDKN1A protein in IP experiments.IP samples: HCT-116 whole cell extract treat with 30uM cisplatin for 48 hrA. 30 ?g HCT-116 whole cell extract treat with 30uM cisplatin for 48 hrB. Control with 4 ?g of preimmu](https://www.grp-ak.de/media/catalog/product/p/2/p21-cip1-antibody-gt1032_grp532_ip_1_2.jpg)
![p21 Cip1 antibody [GT1032] detects p21 Cip1 protein at nucleus by immunofluorescent analysis.Sample: MCF7 cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: CDK4 protein stained by CDK4 antibody (GRP532) diluted at 1:1000.Red: p21 Cip1 protei](https://www.grp-ak.de/media/catalog/product/p/2/p21-cip1-antibody-gt1032_grp532_if_1_2.jpg)
![LC3B antibody [GT3612] detects LC3B protein at autophagosome by immunofluorescent analysis. Samples: HeLa cells mock (left) and treated with 50?M Chloroquine for 24 hr (right) were fixed in 4% paraformaldehyde at RT for 15 min.Green: LC3B protein stained](https://www.grp-ak.de/media/catalog/product/l/c/lc3b-antibody-gt3612_grp533_if_1_2.jpg)
![Untreated (–) and treated (+) HeLa whole cell extracts (50 ?g) were separated by 15% SDS-PAGE, and the membrane was blotted with LC3B antibody [GT3612] (GRP533) diluted at 1:500.](https://www.grp-ak.de/media/catalog/product/l/c/lc3b-antibody-gt3612_grp533_wb_3_2.jpg)
![Untreated (–) and treated (+) HepG2 whole cell extracts (30 ?g) were separated by 15% SDS-PAGE, and the membrane was blotted with LC3B antibody [GT3612] (GRP533) diluted at 1:500.](https://www.grp-ak.de/media/catalog/product/l/c/lc3b-antibody-gt3612_grp533_wb_2_2.jpg)
![Non-transfected (–) and transfected (+) 293T whole cell extracts (30 ?g) were separated by 15% SDS-PAGE, and the membrane was blotted with LC3B antibody [GT3612] (GRP533) diluted at 1:500.](https://www.grp-ak.de/media/catalog/product/l/c/lc3b-antibody-gt3612_grp533_wb_1_2.jpg)
![Immunohistochemical analysis of paraffin-embedded cervical CA tissue sections using anti-CAIX antibody [GT12] (GRP534) at a dilution of 1:1000. The hypoxic regions of the tumor show positive CAIX staining.](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_ihc-p_5_2.jpg)
![Sample (30 μg HeLa whole cell lysate)A: 24 hr UntreatedB: 24 hr treatment with 100μM CoCl2C: 24 hr treatment with 200μM CoCl2D: 48 hr UntreatedE: 48 hr treatment with 100μM CoCl2F: 48 hr treatment with 200μM CoCl2Anti-CAIX antibody [GT12] (](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_wb_1_2.jpg)
![Immunohistochemical analysis of paraffin-embedded cervical CA tissue sections using anti-CAIX antibody [GT12] (GRP534) at a dilution of 1:1000. The hypoxic regions of the tumor show positive CAIX staining.](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_ihc-p_4_2.jpg)
![Confocal immunofluorescence analysis (Olympus FV10i) of methanol-fixed A431 cells treated with 200?M CoCl2 for 48hr using anti-CAIX antibody [GT12] (GRP534) at a dilution of 1:1000.](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_facs_2_2.jpg)
![Flow cytometry on HeLa cells (1x10^6) stained with anti-CAIX antibody [GT12] (GRP534) at a 1:1000 dilution. HeLa cells were untreated (green) or treated with 200?M CoCl2 (pink) for 48 hr.](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_facs_1_2.jpg)
![Immunohistochemical analysis of paraffin-embedded renal cell carcinoma (clear cell type) using anti-CAIX antibody [GT12] (GRP534) at a dilution of 1:1000.](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_ihc-p_3_2.jpg)
![Carbonic Anhydrase IX antibody [GT12] detects Carbonic Anhydrase IX protein at cell membrane by immunohistochemical analysis.Sample: Paraffin-embedded human cervical carcinoma.Carbonic Anhydrase IX stained by Carbonic Anhydrase IX antibody [GT12] (GRP534)](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_ihc-p_2_2.jpg)
![The IHC-P analysis of Carbonic Anhydrase IX antibody [GT12] was published by Huang WJ and colleagues in the journal PLoS One in 2015.PMID: 25738958](https://www.grp-ak.de/media/catalog/product/c/a/carbonic-anhydrase-ix-antibody-gt12_grp534_ihc-p_1_2.jpg)
![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)
![Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with ATR antibody [2B5] (GRP536) diluted at 1:500. The HRP-conjugated anti-mouse IgG antibody was used to detect the](https://www.grp-ak.de/media/catalog/product/a/t/atr-antibody-2b5_grp536_wb_1_2.jpg)
![BRCA1 antibody [17F8] - ChIP grade detects BRCA1 protein by western blot analysis. Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and blotted with BRCA1 antibody [17F8] - ChIP grade (GRP537) diluted by 1:500. The HRP-conjugated anti](https://www.grp-ak.de/media/catalog/product/b/r/brca1-antibody-17f8-chip-grade_grp537_wb_1_2.jpg)
![The IHC-P analysis of BRCA1 antibody [17F8] - ChIP grade was published by Bernard-Gallon DJ and colleagues in the journal Breast Cancer Res in 2001.PMID: 11250747](https://www.grp-ak.de/media/catalog/product/b/r/brca1-antibody-17f8-chip-grade_grp537_ihc-p_2_2.jpg)
![The IHC-P analysis of BRCA1 antibody [17F8] - ChIP grade was published by Bernard-Gallon DJ and colleagues in the journal Breast Cancer Res in 2001.PMID: 11250747](https://www.grp-ak.de/media/catalog/product/b/r/brca1-antibody-17f8-chip-grade_grp537_ihc-p_1_2.jpg)
![BRCA1 antibody [6B4] (GRP538) was used at 1:1000 dilution for western blot assay of lysates from cells transfected with control or BRCA1-specific siRNA. Lysates were prepared at the indicated times following transfection. RAD50 antibody [13B3] (GRP538) wa](https://www.grp-ak.de/media/catalog/product/b/r/brca1-antibody-6b4-chip-grade_grp538_wb_2_2.jpg)
