HSD17B2 Antibody – Rabbit Polyclonal

Figure 1. Western blot analysis of HSD17B2 using anti-HSD17B2 antibody (MBS1753530).
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: human placenta 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-HSD17B2 antigen affinity purified polyclonal antibody (Catalog # MBS1753530) 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 HSD17B2 at approximately 40KD. The expected band size for HSD17B2 is at 40KD.

Figure 2. Flow Cytometry analysis of CACO-2 cells using anti-HSD17B2 antibody (MBS1753530).
Overlay histogram showing CACO-2 cells stained with MBS1753530 (Blue line). The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSD17B2 Antibody (MBS1753530, 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.