Western blot (WB): | 1:500-2000 |
Flow Cytometry (Fixed): | 1:50-200 |
Western blot analysis of CCR5 using anti-CCR5 antibody (BA0376-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Jurkat whole cell lysates,
Lane 2: Jurkat whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CCR5 antigen affinity purified polyclonal antibody (BA0376-2) 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 CCR5 at approximately 40 kDa. The expected band size for CCR5 is at 41 kDa.
Flow cytometry analysis of human PBMC cell(1:100) DyLight 488 conjugated goat anti-rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).
Western blot analysis of CCR5 using anti-CCR5 antibody (BA0376-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Jurkat whole cell lysates,
Lane 2: Jurkat whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CCR5 antigen affinity purified polyclonal antibody (BA0376-2) 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 CCR5 at approximately 40 kDa. The expected band size for CCR5 is at 41 kDa.
Flow cytometry analysis of human PBMC cell(1:100) DyLight 488 conjugated goat anti-rabbit IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG DyLight 488. Unlabelled sample (Red line).