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应用
Biliverdin Reductase Assay Kit contains all the reagents necessary for activity detection of biliverdin reductase. The formation of bilirubin from biliverdin is followed by a colorimetric reaction at 450 nm, in an NADPH dependent reaction, at pH 8.5 at 37 °C. The kit was tested on tissue extracts prepared from rat liver, brain, heart, spleen, lung, skeletal muscle, and kidney. It was also tested on HEK-293T, BAEC, HepG2, COS, Jurkat, Balb/3T3, CHO, and U937 cell lines.
生化/生理作用
Biliverdin reductase (BVR) catalyzes the transformation of the blue-green pigment biliverdin IX to the yellow-orange bile pigment, bilirubin IX. A major feature of this enzyme is that it is the only enzyme shown to have two distinct cofactor dependent pH optima. In the acidic range of pH 6.0-6.7, NADH is utilized; whereas, in the alkaline range of pH 8.5-8.7, NADPH is used. Biliverdin reductase is also known to contain a domain that acts as a serine/threonine/tyrosine kinase that belongs to the insulin receptor substrate family. Whereas, most tyrosine kinase activity is membrane bound, BVR is a soluble protein.
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产品编号
说明
化学品安全说明书
- N6505β-Nicotinamide adenine dinucleotide 2′-phosphate reduced tetrasodium salt hydrate, ≥95% (HPLC) 100 mg化学品安全说明书
法规信息
新产品
Physiology (Bethesda, Md.), 20, 382-389 (2005-11-17)
Biliverdin reductase (BVR) functions in cell signaling through three distinct tracks: a dual-specificity kinase that functions in the insulin receptor/MAPK pathways (25, 29, 51); a bzip-type transcription factor for ATF-2/CREB and HO-1 regulation (1, 25); and a reductase that catalyzes
The Journal of biological chemistry, 256(8), 3956-3962 (1981-04-25)
Biliverdin reductase in a stable form was purified to homogeneity from rat liver cytosol. The purified enzyme showed 3700-fold increase in specific activity when compared with the crude preparation, and the extent of recovery was 30-35%. The molecular weight was
Biliverdin reductase of guinea pig liver.
The Journal of biological chemistry, 240(12), 4780-4789 (1965-12-01)
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