Antibodies

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Western blot analysis on NIH-3T3 cell lysate using MLANA Antibody. The lane on the left is treated with the antigen-specific peptide.AF0204 staining NIH-3T3 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
Affinity Biosciences MLANA Antibody
From $537.37
Western blot analysis on HepG2 cell lysate using Mammaglobin B Antibody. The lane on the left is treated with the antigen-specific peptide.AF0203 at 1/100 staining human colon carcinoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Mammaglobin B Antibody
From $537.37
AF0202 at 1/100 staining human breast carcinoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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 secondaryAF0202 staining HeLa cells 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) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibod
Affinity Biosciences Mammaglobin Antibody
From $537.37
Western blot analysis on HeLa cell lysate using Ku70 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0201 at 1/100 staining human brain tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Ku70 Antibody
From $537.37
Western blot analysis on COS7 cell lysate using Ku80 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0200 at 1/100 staining human colon carcinoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Ku80 Antibody
From $537.37
AF0199 at 1/200 staining human kidney tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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 secondaryAF0199 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
Affinity Biosciences iNOS Antibody
From $537.37
This image is a courtesy of anonymous review.Western blot analysis of extracts of various tissue sample,using ki67 antibody.
Affinity Biosciences Ki67 Antibody
From $537.37
Western blot analysis of extracts of various tissue ,using Keratin 10 antibody.AF0197 staining HeLa 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
Affinity Biosciences Keratin 10 Antibody
From $537.37
Western blot analysis on 293 cell lysate using Keratin 8 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0196 at 1/100 staining human kidney tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Keratin 8 Antibody
From $537.37
Western blot analysis on HepG2 cell lysate using Keratin 7 AntibodyAF0195 staining Hela by IF/ICC. The samples were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25¡ãC. Samples were then incubated with primary Ab(AF0195 1:200) and mouse anti-beta tubulin Ab(T0023 1:200) for 1 hour at 37¡ãC. An AlexaFluor594 conjugated goat anti-rabbit IgG(H+L) Ab(S0006 1:200 Red) and an AlexaFluor488 conjugated goat anti-mouse IgG(H+L) Ab(S0017 1:600 Green) were used as the secondary antibod
Affinity Biosciences Keratin 7 Antibody
From $537.37
Western blot analysis on HepG2 cell lysate using Keratin 5 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0194 at 1/100 staining human colon 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
Affinity Biosciences Keratin 5 Antibody
From $537.37
Western blot analysis on HeLa cell lysate using Keratin 20 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0193 at 1/200 staining human colon carcinoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Keratin 20 Antibody
From $537.37
Western blot analysis on LOVO cell lysate using Keratin 19 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0192 at 1/500 staining human colon cancer tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Keratin 19 Antibody
From $537.37
AF0191 at 1/200 staining human kidney tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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 secondaryAF0191 staining HT29 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
Affinity Biosciences Keratin 18 Antibody
From $537.37
Western blot analysis on HuvEc cell lysate using Keratin 17 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0190 at 1/200 staining human kidney tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Keratin 17 Antibody
From $537.37
Western blot analysis on HepG2 cell lysate using Keratin 16 Antibody. The lane on the left is treated with the antigen-specific peptide.AF0189 at 1/200 staining human skin carcinoma tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences Keratin 16 Antibody
From $537.37
Western blot analysis of JM4 expression in Rat liver lysateWestern blot analysis of JM4 expression in mouse brain lysate
Affinity Biosciences JM4 Antibody
From $537.37
AF0187 staining A549? cells 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) antibody(Cat.# S0006), diluted at 1/600, was used as secondary antibodAF0187 staining LOVO 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
Affinity Biosciences COPS3 Antibody
From $537.37
IHC analysis of mouse brain tissue.AF0186 staining HuvEc 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
Affinity Biosciences Involucrin Antibody
From $537.37
Western blot analysis on mouse brain lysate using Integrin beta-5 Antibody.AF0185 staining Hela 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
Affinity Biosciences Integrin beta-5 Antibody
From $537.37
western blot analyses for the mRNA and protein expression of Hsp60 in tumor and paired peritumor tissues from HCC patients. Quantitative analysis of protein levels was performed by measuring the ratio of Hsp60 to ?-actin expression. Error bars indicate SD.*P<0.05.Immunofluorescence analysis of the Hsp60 expression in BEL-7402 cell (Scale bars, 10?m).
Affinity Biosciences HSP60 Antibody
From $537.37
Western blot analysis on NIH-3T3 cell lysate using HSP10 Antibody,The lane on the left is treated with the antigen-specific peptide.AF0183 at 1/100 staining human kidney tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences HSP10 Antibody
From $537.37
AF0182 at 1/100 staining human brain tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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 secondaryAF0182 staining SKOV3 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
Affinity Biosciences NRG1 isoform-10 Antibody
From $537.37
Western blot analysis on HepG2 cell lysate using HDAC9 Antibody,The lane on the left is treated with the antigen-specific peptide.AF0181 at 1/100 staining human brain tissue sections by IHC-P. The tissue was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The tissue 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
Affinity Biosciences HDAC9 Antibody
From $537.37

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