Application Notes: WB: human MCF-7 whole cell, human Hela whole cell, human HepG2 whole cell, rat kindey tissue, mouse pancreas tissue, mouse kindey tissue. IHC: human gall bladder adenosquamous carcinoma tissue, human hyroid papillary carcinoma tissue, human liver cancer tissue, mouse colon tissue, mouse brain tissue, rat brain tissue. ICC/IF: CACO-2 cell
Western blot analysis of GPR54/KISS1R using antiGPR54/KISS1R antibody. Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat kindey tissue lysates, Lane 5: mouse pancreas tissue lysates, Lane 6: mouse kindey tissue lysates.
IHC analysis of GPR54/KISS1R using anti-GPR54/KISS1R antibody. GPR54/KISS1R was detected in a paraffin-embedded section of human gall bladder adenosquamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-GPR54/KISS1R Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen
IHC analysis of GPR54/KISS1R using anti-GPR54/KISS1R antibody. GPR54/KISS1R was detected in a paraffin-embedded section of human hyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-GPR54/KISS1R Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen
IHC analysis of GPR54/KISS1R using anti-GPR54/KISS1R antibody. GPR54/KISS1R was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-GPR54/KISS1R Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen
IHC analysis of GPR54/KISS1R using anti-GPR54/KISS1R antibody. GPR54/KISS1R was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-GPR54/KISS1R Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex with DAB as the chromogen
IHC analysis of GPR54/KISS1R using anti-GPR54/KISS1R antibody. GPR54/KISS1R was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-GPR54/KISS1R Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen
IHC analysis of GPR54/KISS1R using anti-GPR54/KISS1R antibody. GPR54/KISS1R was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-GPR54/KISS1R Antibody overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary
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