WB
Western blot analysis of RAB27A+RAB27B on different lysates with Rabbit anti-RAB27A+RAB27B antibody at 1/5,000 dilution.
Lysates/proteins at 15 µg/Lane.
Exposure time: 10 seconds;
Negative control: Raji.
Blocking: 5% NFDM/TBST, 1 hour at room temperature.
Primary antibody: RAB27A+RAB27B Recombinant Rabbit Monoclonal Antibody, 1/5,000 in primary antibody dilution buffer, overnight at 4 ℃.
Secondary antibody: Goat anti-Rabbit IgG-HRP, 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature.
FC
Application: Flow Cytometry (Intra).
Species: Rat.
Sample: PC-12 (Rat pheochromocytoma cells (undifferentiated)).
Fixation: 4% Paraformaldehyde, 15 minutes at room temperature.
Permeabilization: 1x Permeabilization Buffer (eBioscience), 15 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 15 minutes at room temperature.
Antibody dilution buffer: 1x PBS.
Primary antibody: RAB27A+RAB27B Recombinant Rabbit Monoclonal Antibody(1/1,000, Red) compared with Rabbit IgG Isotype Control (Green), 15 minutes at room temperature.
Secondary antibody: Goat Anti-Rabbit IgG (488), 15 minutes at room temperature.
IP
Immunoprecipitation (IP).
RAB27A+RAB27B was immunoprecipitated in 0.2 mg K-562 (Human chronic myelogenous leukemia cell) cell lysate with RAB27A+RAB27B Recombinant Rabbit Monoclonal Antibodyat 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using RAB27A+RAB27B Recombinant Rabbit Monoclonal Antibodyat 1/5,000 dilution. Alpaca anti-Rabbit IgG Fc, Recombinant VHH monoclonal Antibody at 1/50000 dilution was used for 1 hour at room temperature.
Lane 1: K-562 cell lysate (input).
Lane 2: RAB27A+RAB27B Recombinant Rabbit Monoclonal Antibody IP in K-562 cell lysate.
Lane 3: Rabbit IgG instead of RAB27A+RAB27B Recombinant Rabbit Monoclonal Antibody in K-562 cell lysate.
Exposure time: 2 seconds.
Blocking: 5% NFDM/TBST, 1 hour at room temperature.
Primary dilution: RAB27A+RAB27B Recombinant Rabbit Monoclonal Antibody, 1/5,000 in primary antibody dilution buffer, 2 hours at room temperature.