Antibodies

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Western blot analysis of ABHD10 using 293 whole cell lysates
Western blot analysis of ABHD1 using K562 whole cell lysates
Western blot analysis INPP5E using K562 whole cell lysates
Western blot analysis NIP7 using LOVO whole cell lysates
Western blot analysis of RPL7A using K562 whole cell lysates
Western blot analysis of RPL41 using Jurkat whole cell lysates
DF9135 at 1/100 staining Mouse liver 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 RPL38 using COS7 whole cell lysates
Western blot analysis of extracts from Rat spleen, using RPL37 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of RPL36L using HuvEc whole cell lysates
Western blot analysis of RPL35A using A549 whole cell lysates
Western blot analysis of extracts from various samples, using RPL29 Antibody.
 Lane 1: Mouse Myeloma cell treated with blocking peptide.
 Lane 2: Mouse Myeloma cell;
 Lane 3: Hela;
Western blot analysis of RPL27 using COLO205 whole cell lysates
Western blot analysis of extracts from various samples, using RPL24 Antibody.
 Lane 1: Mouse Myeloma cell treated with blocking peptide.
 Lane 2: Mouse Myeloma cell;
 Lane 3: Hela;
 Lane 4: huvel;
DF9127 at 1/100 staining Human prostate 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 RPL13A using COS7 whole cell lysates
Western blot analysis of RPLP1 using COLO205 whole cell lysates
DF9124 at 1/100 staining Human prostate 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
DF9123 at 1/100 staining Rat heart 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
DF9122 at 1/100 staining Rat liver 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 RPS26L1 using HeLa whole cell lysates
Western blot analysis of RPS24 using HepG2 whole cell lysates
Western blot analysis of RPS21 using Jurkat whole cell lysates
Western blot analysis of RPS17 using Jurkat whole cell lysates

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