Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
ELISA(Cap): | 1:50-1:200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Western blot analysis of VCAM1 using anti-VCAM1 antibody (A01199). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: mouse spleen tissue lysates,
Lane 2: mouse lung tissue lysates,
Lane 3: rat spleen tissue lysates,
Lane 4: rat lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-VCAM1 antigen affinity purified polyclonal antibody (A01199) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for VCAM1 at approximately 85-110 kDa. The expected band size for VCAM1 is at 81 kDa.
IHC analysis of VCAM1 using anti-VCAM1 antibody (A01199).
VCAM1 was detected in a paraffin-embedded section of mouse spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-VCAM1 Antibody (A01199) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of VCAM1 using anti-VCAM1 antibody (A01199).
VCAM1 was detected in a paraffin-embedded section of rat spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-VCAM1 Antibody (A01199) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Western blot analysis of VCAM1 using anti-VCAM1 antibody (A01199). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: mouse spleen tissue lysates,
Lane 2: mouse lung tissue lysates,
Lane 3: rat spleen tissue lysates,
Lane 4: rat lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-VCAM1 antigen affinity purified polyclonal antibody (A01199) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for VCAM1 at approximately 85-110 kDa. The expected band size for VCAM1 is at 81 kDa.
IHC analysis of VCAM1 using anti-VCAM1 antibody (A01199).
VCAM1 was detected in a paraffin-embedded section of mouse spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-VCAM1 Antibody (A01199) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of VCAM1 using anti-VCAM1 antibody (A01199).
VCAM1 was detected in a paraffin-embedded section of rat spleen tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-VCAM1 Antibody (A01199) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.