COX8A Antibody – Rabbit Polyclonal

Figure 1. Western blot analysis of COX8A using anti-COX8A antibody (MBS1753830).
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 50ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates
Lane 2: rat stomach tissue lysates
Lane 3: rat kidney tissue lysates
Lane 4: mouse brain tissue lysates
Lane 5: mouse kidney tissue lysates.
After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA for 50-90 minutes. Blocked the membrane with 5% Non-fat Milk/ TBS for 1. 5 hour at RT. The membrane was incubated with rabbit anti-COX8A antigen affinity purified polyclonal antibody (Catalog # MBS1753830) at 0. 5 μg/mL overnight at 4 degree C, then washed with TBS-0. 1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1. 5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # MBS176460) with Tanon 5200 system. A specific band was detected for COX8A at approximately 8-10KD. The expected band size for COX8A is at 8-10KD.

Figure 2. Flow Cytometry analysis of mouse spleen tissues using anti-COX8A antibody (MBS17538302).
Overlay histogram showing mouse spleen tissues stained with MBS1753830 (Blue line). The tissues were blocked with 10% normal goat serum. And then incubated with rabbit anti-COX8A Antibody (MBS1753830, 1μg/1x10⁶ cells) for 30 min at 20 degree C. DyLight®488 conjugated goat anti-rabbit IgG (5-10μg/1x10⁶ cells) was used as secondary antibody for 30 minutes at 20 degree C. Isotype control antibody (Green line) was rabbit IgG (1μg/1x10⁶) used under the same conditions. Unlabelled sample (Red line) was also used as a control.

Figure 3. IHC analysis of COX8A using anti-COX8A antibody (MBS1753830).
COX8A was detected in paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8. 0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-COX8A Antibody (MBS1753830) overnight at 4 degree C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 degree C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # MBS176451) with DAB as the chromogen.