Antibodies

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Western blot analysis of hnRNP A0 using COLO205 whole cell lysates
Western blot analysis of extracts from mouse brain, using ZBTB17 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of COASY using COS7 whole cell lysates
DF8820 at 1/100 staining Mouse muscle tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis of TAF10 using Jurkat whole cell lysates
Western blot analysis FOXI1 using HuvEc whole cell lysates
Western blot analysis of EGR3 using K562 whole cell lysates
Western blot analysis of extracts from Hybridoma cells, using WIT1 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of EMX2 using K562 whole cell lysates
DF8814 at 1/100 staining Mouse spleen tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis of AKAP12 using Jurkat whole cell lysates
DF8812 at 1/100 staining Human gastric tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
DF8811 at 1/100 staining Mouse lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis of extracts from various samples, using SERF2 Antibody.
 Lane 1: Hela treated with blocking peptide;
 Lane 2: Hela;
 Lane 3: HepG2.
Western blot analysis of MRPS11 using MCF7 whole cell lysates
DF8984 at 1/100 staining Human Melanoma tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis IL26 using COS7 whole cell lysates
Western blot analysis IL19 using HeLa whole cell lysates
DF8981 at 1/100 staining Human Melanoma tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
DF8980 at 1/100 staining Human Melanoma tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
DF8979 at 1/100 staining Mouse testis tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis IRGC using HeLa whole cell lysates
Western blot analysis of extracts from Mouse  brain, using IGFL3 Antibody. The lane on the left was treated with blocking peptide.

Observed bands: 20 kDa.
Western blot analysis IFIT1B using COLO205 whole cell lysates

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