Search results for: 'Cholera Toxin - 7953 - B subunit, 1 mg'
-                 E(z) - Histone-lysine N-methyltransferase E(z) [GRP13163]ChIP, IP Drosophila Rabbit Polyclonal 50 µg
-                 ASH1 - Histone-lysine N-methyltransferase ASH1 [GRP12973]ChIP, IL Drosophila Rabbit Polyclonal 50 µg
-                 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
-                 Transcription Initiation Factor TFIID Subunit 1 (TAF1) (RABBIT) Antibody [GRP3583]ChIP, ELISA, IHC-P, IP, WB Human, Mouse Rabbit Polyclonal 100ug
-                 HIF1 alpha antibody [GRP65]ChIP, ICC, IF, IHC-Fr, IHC-P, IP, WB Human, Mouse, Rat, Bovine, Rabbit Rabbit Polyclonal 100 μl
-                 PARP antibody [GRP12]ChIP, ICC, IF, IHC-Fr, IHC-P, IP, WB Human, Mouse, Rat Rabbit Polyclonal 100 μl
-                 PARP antibody [N2C1], Internal [GRP54]ChIP, ICC, IF, IHC-P, IP, WB Human, Mouse, Rat Rabbit Polyclonal 100 μl
-                 TET1 antibody [N3C1] [GRP63]ChIP, ICC, IF, IHC-P, IP, WB Human, Mouse, Monkey Rabbit Polyclonal 100 μl
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                                        ![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) 
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                         
                                        ![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) 
                                        ![Various whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with TET1 antibody [N3C1] (GRP515) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody  was used to detect the primary antibody.](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-n3c1_grp515_wb_3_2.jpg) 
                                        ![TET1 antibody [N3C1] detects TET1 protein at nucleus in human A549 xenograft by immunohistochemical analysis. Sample: Paraffin-embedded human A549 xenograft . TET1 antibody [N3C1] (GRP515) diluted at 1:250.](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-n3c1_grp515_ihc-p_1_2.jpg) 
                                        ![TET1 antibody [N3C1] detects TET1 protein at nucleus on Human normal prostate tissue by immunohistochemical analysis. Sample: Paraffin-embedded Human normal prostate tissue. TET1 antibody [N3C1] (GRP515) dilution: 1:1000.](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-n3c1_grp515_ihc_2_2.jpg) 
                                        ![HeLa whole cell and nuclear extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with TET1 antibody [N3C1] (GRP515) 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/t/e/tet1-antibody-n3c1_grp515_wb_2_2.jpg) 
                                        ![TET1 antibody [N3C1] detects TET1 protein at nucleus by immunofluorescent analysis.Sample: Mock and transfected 293T cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: TET1 stained by TET1 antibody [N3C1] (GRP515) diluted at 1:1000.Blue: Hoec](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-n3c1_grp515_icc_1_2.jpg) 
                                        ![TET1 antibody [N3C1] detects TET1 protein by western blot analysis.A. 30 μg 293T whole cell lysate/extractB. 30 μg whole cell lysate/extract of DDDDK-human TET1-transfected 293T cells5% SDS-PAGETET1 antibody [N3C1] (GRP515) dilution: 1:5000 The HRP-](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-n3c1_grp515_wb_1_2.jpg) 
                                         
                                        ![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) 
                                        