Antibodies

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Western blot analysis of MEGF6 using Jurkat whole cell lysates
DF9643 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 MUC7 using K562 whole cell lysates
Western blot analysis of MUC6 using COLO205 whole cell lysates
Western blot analysis of MUC5B using COLO205 whole cell lysates
Western blot analysis of MUC5A using Jurkat whole cell lysates
Western blot analysis of MUC4 using Jurkat whole cell lysates
Western blot analysis of extracts from 3t3, using MPHOSPH8 Antibody. The lane on the left was treated with blocking peptide.
DF9636 at 1/100 staining Human liver cancer 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
DF9635 at 1/100 staining Human liver cancer 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 mouse brain, using MOT6 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of MOT2 using COS7 whole cell lysates
Western blot analysis of extracts from hybridoma cells, using MOT11 Antibody. Lane 1 was treated with the blocking peptide.
DF9631 at 1/100 staining Mouse kidney 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 IMMP2L Antibody.
 Lane 1: 3t3 treated with blocking peptide;
 Lane 2: 3t3;
 Lane 3: Mouse muscle.
Western blot analysis IMMP1L using 293 whole cell lysates
Western blot analysis of MRPL33 using COS7 whole cell lysates
Western blot analysis of MRPL27 using HuvEc whole cell lysates
Western blot analysis of extracts from hybridoma cells, using MRPL23 Antibody. Lane 1 was treated with the blocking peptide.
Western blot analysis of MRPS28 using HepG2 whole cell lysates
Western blot analysis of extracts from 3t3, using MID1IP1 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of MAP1A using COLO205 whole cell lysates
Western blot analysis of MIA3 using Jurkat whole cell lysates
DF9621 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

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