Antibodies

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Western blot analysis of PSMD13 using MCF7 whole cell lysates
Western blot analysis of AGPAT7 using HT29 whole cell lysates
Western blot analysis of AGPAT1 using 293 whole cell lysates
Western blot analysis SOX17 using LOVO whole cell lysates
DF9089 at 1/100 staining Mouse pancreas 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
DF9088 at 1/100 staining Rat 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 ORC6L using COLO205 whole cell lysates
Western blot analysis ORC4L using K562 whole cell lysates
DF9085 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
Western blot analysis of extracts from Hepg2, using FMR1NB Antibody. Lane 1 was treated with the blocking peptide.
DF9083 at 1/100 staining Human brain 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 SP6 using COS7 whole cell lysates
Western blot analysis SP5 using LOVO whole cell lysates
DF9080 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 of MAF1 using RAW264.7 whole cell lysates
Western blot analysis of KLF16 using RAW264.7 whole cell lysates
Western blot analysis GEMIN8 using K562 whole cell lysates
Western blot analysis of ERCC2 using A549 whole cell lysates
Western blot analysis of BCL6B using COLO205 whole cell lysates
Western blot analysis of extracts from VERO, using ALKBH7 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of ALKBH2 using HT29 whole cell lysates
Western blot analysis of ACTL6B using HeLa whole cell lysates
Western blot analysis of extracts from various samples, using GOLT1B Antibody.
 Lane 1: mouse brain treated with blocking peptide.
 Lane 2: mouse brain;
 Lane 3: rat brain;
Western blot analysis of CREB3L4 using K562 whole cell lysates

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