Search results for: 'anti dengue ns1'
- 10 imagesFibronectin antibody [N1N2], N-term [GRP53]
ELISA, 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 -
- 3 images
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- 10 images
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- 4 images
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- 5 images
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- 4 images
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- 3 images
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- 10 imagesAKT antibody [N3C2], Internal [GRP61]
ICC, IF, IHC-Fr, IHC-P, IP, WB
Human, Mouse, Rat, Fish
Rabbit
Polyclonal
100 μl -
- 6 images
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![Fibronectin antibody [N1N2], N-term detects FN1 protein at cytosol on human hepatoma by immunohistochemical analysis. Sample: Paraffin-embedded hepatoma. Fibronectin antibody [N1N2], N-term (GRP505) dilution: 1:500.](https://www.grp-ak.de/media/catalog/product/f/i/fibronectin-antibody-n1n2-n-term_grp505_ihc_1_2.jpg)
![Indirect ELISA analysis was performed by coating plate with 100 μL of recombinant Fibronectin protein at concentration of 10 μg/mL. The coated protein is detected with Fibronectin antibody [N1N2], N-term (GRP505) at rangeing from 0.5 to 140 ng/mL.](https://www.grp-ak.de/media/catalog/product/f/i/fibronectin-antibody-n1n2-n-term_grp505_elisa_2_2.jpg)
![Fibronectin antibody [N1N2] detects Fibronectin protein by western blot analysis. Mouse tissue extracts (50 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with Fibronectin antibody [N1N2] (GRP505) diluted at 1:1000. The HRP-conjugated a](https://www.grp-ak.de/media/catalog/product/f/i/fibronectin-antibody-n1n2-n-term_grp505_wb_4_2.jpg)
![Untreated (–) and treated (+) HepG2 whole cell extracts (30 μg) were separated by 5% SDS-PAGE, and the membrane was blotted with Fibronectin antibody [N1N2], N-term (GRP505) diluted at 1:2000. The HRP-conjugated anti-rabbit IgG antibody was used to](https://www.grp-ak.de/media/catalog/product/f/i/fibronectin-antibody-n1n2-n-term_grp505_wb_3_2.jpg)
![The WB analysis of Fibronectin antibody [N1N2], N-term was published by Pon JR and colleagues in the journal Nat Commun in 2015.PMID: 26245647](https://www.grp-ak.de/media/catalog/product/f/i/fibronectin-antibody-n1n2-n-term_grp505_wb_2_2.jpg)
![The WB analysis of Fibronectin antibody [N1N2], N-term was published by Pon JR and colleagues in the journal Nat Commun in 2015.PMID: 26245647](https://www.grp-ak.de/media/catalog/product/f/i/fibronectin-antibody-n1n2-n-term_grp505_wb_1_2.jpg)
![Fibronectin antibody [N1N2], N-term immunoprecipitates Fibronectin protein in IP experiments. IP Sample: HeLa whole cell lysate/extract A : 30 ?g whole cell lysate/extract of Fibronectin protein expressing HeLa cells B : Control with 3 ?g of pre-immune ra](https://www.grp-ak.de/media/catalog/product/f/i/fibronectin-antibody-n1n2-n-term_grp505_ip_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)
![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)
