SNRK Antilichaam/SNF-gerelateerd serine/threonine-eiwitkinase

Western Blot: 0.25-0.5 µg/mL, ELISA: 0.1-0.5 µg/mL

Q9NRH2

Human, Mouse, Rat

E.coli-derived human SNRK recombinant protein (Position: D48-E750) was used as the immunogen for the SNRK antibody.

WB, ELISA

Immunogen affinity purified

Lyophilized

Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

This SNRK antibody is available for research use only.

After reconstitution, the SNRK antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Adding 0.2 ml of distilled water will yield a concentration of 500 ug/ml

Optimal dilution of the SNRK antibody should be determined by the researcher.

Western blot analysis of SNRK using anti-SNRK antibody. Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. Lane 1: human Jurkat whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA 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-SNRK antibody at 0.5 ug/ml overnight at 4oC, 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 was developed using an ECL Plus Western Blotting Substrate. A predominant band is detected between an approximately 75 and 80 kDa in all samples, slightly below the predicted ~84 kDa size but consistent with the apparent molecular weight of the major SNRK isoform under these electrophoresis conditions.