Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:1000-5000 |
Immunofluorescence (IF): | 1:50-400 |
Western blot analysis of anti- GFAP antibody (BM0055). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: U251 whole cell lysates,
Lane 2: rat brain tissue lysates,
Lane 3: rat C6 whole cell lysates,
Lane 4: mouse brain tissue lysates.
Use mouse anti- GFAP 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for GFAP at approximately 50KD. The expected band size for GFAP is at 54KD.
IHC analysis using anti- GFAP antibody (BM0055). detected in paraffin-embedded section of rat brain tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
IF analysis of GFAP, MBP using anti- GFAP antibody(BM0055), anti- MBP antibody(BA0094),detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL mouse anti-GFAP, DyLight488 Conjugated Goat Anti-Mouse IgG (BA1126), rabbit anti-MBP Antibody , Cy3 Conjugated goat anti-rabbit IgG (BA1032) overnight at 4°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
Western blot analysis of anti- GFAP antibody (BM0055). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: U251 whole cell lysates,
Lane 2: rat brain tissue lysates,
Lane 3: rat C6 whole cell lysates,
Lane 4: mouse brain tissue lysates.
Use mouse anti- GFAP 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for GFAP at approximately 50KD. The expected band size for GFAP is at 54KD.
IHC analysis using anti- GFAP antibody (BM0055). detected in paraffin-embedded section of rat brain tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
IF analysis of GFAP, MBP using anti- GFAP antibody(BM0055), anti- MBP antibody(BA0094),detected in paraffin-embedded section of rat brain tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL mouse anti-GFAP, DyLight488 Conjugated Goat Anti-Mouse IgG (BA1126), rabbit anti-MBP Antibody , Cy3 Conjugated goat anti-rabbit IgG (BA1032) overnight at 4°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.