Antibodies
- 10 imagesAKT antibody [N3C2], Internal [GRP61]
ICC, IF, IHC-Fr, IHC-P, IP, WB
Human, Mouse, Rat, Fish
Rabbit
Polyclonal
100 μl -
- 7 imagesTET1 antibody [N3C1] [GRP63]
ChIP, ICC, IF, IHC-P, IP, WB
Human, Mouse, Monkey
Rabbit
Polyclonal
100 μl -
- 3 images
-
- 28 imagesHIF1 alpha antibody [GRP65]
ChIP, ICC, IF, IHC-Fr, IHC-P, IP, WB
Human, Mouse, Rat, Bovine, Rabbit
Rabbit
Polyclonal
100 μl -
- 9 imagesHistone H2A.XS139ph (phospho Ser139) antibody [GRP67]
ICC, IF, IHC-P, WB
Human, Mouse, Rat, Zebrafish
Rabbit
Polyclonal
100 μl -
- 8 images
-
- 15 imagesLC3B antibody [GRP69]
FACS, ICC, IF, IHC-Fr, IHC-P, IP, WB
Human, Mouse, Rat, Pig
Rabbit
Polyclonal
100 μl -
- 14 images
-
- 10 imagesAKT (phospho Ser473) antibody [GRP71]
ICC, IF, IHC-P, IP, WB
Human, Mouse, Rat
Rabbit
Polyclonal
100 μl -
- 4 imagesCarbonic Anhydrase IX antibody [GRP72]
ICC, IF, IHC-Fr, IHC-P, WB
Human, Mouse
Rabbit
Polyclonal
100 μl -
![Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with AKT antibody [N3C2], Internal (GRP513) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used](https://www.grp-ak.de/media/catalog/product/a/k/akt-antibody-n3c2-internal_grp513_wb_6_2.jpg)
![Various whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with AKT antibody [N3C2], Internal (GRP513) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and t](https://www.grp-ak.de/media/catalog/product/a/k/akt-antibody-n3c2-internal_grp513_wb_4_2.jpg)
![AKT antibody [N3C2], Internal detects AKT protein at cytoplasm by immunofluorescent analysis.Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: AKT stained by AKT antibody [N3C2], Internal (GRP513) diluted at 1:500.Blue: Hoechst](https://www.grp-ak.de/media/catalog/product/a/k/akt-antibody-n3c2-internal_grp513_icc_1_2.jpg)
![Various whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with AKT antibody [N3C2], Internal (GRP513) 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/a/k/akt-antibody-n3c2-internal_grp513_wb_3_2.jpg)
![The WB analysis of AKT antibody [N3C2], Internal was published by Sun W and colleagues in the journal Cell Death Dis in 2014 .](https://www.grp-ak.de/media/catalog/product/a/k/akt-antibody-n3c2-internal_grp513_wb_2_2.jpg)
![The WB analysis of AKT antibody [N3C2], Internal was published by Vallejo-Flores G and colleagues in the journal Biomed Res Int in 2015.PMID: 26557697](https://www.grp-ak.de/media/catalog/product/a/k/akt-antibody-n3c2-internal_grp513_wb_1_2.jpg)
![Immunoprecipitation of Akt1/2/3 protein from 293T whole cell extracts using 5 ?g of Akt1/2/3 antibody [N3C2], Internal (GRP513).Western blot analysis was performed using Akt1/2/3 antibody [N3C2], Internal (GRP513).EasyBlot anti-Rabbit IgG was used as a s](https://www.grp-ak.de/media/catalog/product/a/k/akt-antibody-n3c2-internal_grp513_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 [N1], N-term detects TET1 protein at nucleus by immunofluorescent analysis.Sample: HepG2 cells were fixed in 4% paraformaldehyde at RT for 15 min.Green: TET1 protein stained by TET1 antibody [N1], N-term (GRP516) diluted at 1:500.Blue: Hoech](https://www.grp-ak.de/media/catalog/product/t/e/tet1-antibody-n1-n-term_grp516_if_1_2.jpg)
