Antibodies

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Western blot analysis UBE4B using Jurkat whole cell lysates
Western blot analysis UBE4A using HepG2 whole cell lysates
Western blot analysis USP6 using HeLa whole cell lysates
Western blot analysis of extracts from mouse muscle and mouse brain, using USP51 Antibody.
DF9993 at 1/100 staining Human 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
DF9992 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 USP35 using COS7 whole cell lysates
Western blot analysis USP34 using HT29 whole cell lysates
DF9989 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
DF9988 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
DF9987 at 1/100 staining Rat brain 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 USP26 using HuvEc whole cell lysates
Western blot analysis USP24 using Jurkat whole cell lysates
Western blot analysis of extracts from mouse brain, using USP17L Antibody.
DF9983 staining HepG2 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37¡ãC. An  Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibod
Western blot analysis USP14 using Jurkat whole cell lysates
Western blot analysis USP12 using K562 whole cell lysates
Western blot analysis UBQLN2 using HeLa whole cell lysates
Western blot analysis of LSM2 using Jurkat whole cell lysates
DF9978 at 1/100 staining Human breast 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 MPHOSPH10 using Jurkat whole cell lysates
Western blot analysis of TNNT1 using HepG2 whole cell lysates
Western blot analysis of extracts from mouse brain, using TMC7 Antibody.
Western blot analysis of BTF3L4 using HT29 whole cell lysates

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