|Calculated MW||37 KDa|
|Other Names||Aldo-keto reductase family 1 member C2, 1.-.-.-, 3-alpha-HSD3, Chlordecone reductase homolog HAKRD, Dihydrodiol dehydrogenase 2, DD-2, DD2, Dihydrodiol dehydrogenase/bile acid-binding protein, DD/BABP, Trans-1, 2-dihydrobenzene-1, 2-diol dehydrogenase, 188.8.131.52, Type III 3-alpha-hydroxysteroid dehydrogenase, 184.108.40.2067, AKR1C2, DDH2|
|Format||Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol|
|Storage||Store at -20 °C.Stable for 12 months from date of receipt|
|Function||Works in concert with the 5-alpha/5-beta-steroid reductases to convert steroid hormones into the 3-alpha/5-alpha and 3-alpha/5-beta-tetrahydrosteroids. Catalyzes the inactivation of the most potent androgen 5-alpha-dihydrotestosterone (5-alpha- DHT) to 5-alpha-androstane-3-alpha,17-beta-diol (3-alpha-diol). Has a high bile-binding ability.|
|Tissue Location||Expressed in fetal testes. Expressed in fetal and adult adrenal glands.|
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Works in concert with the 5-alpha/5-beta-steroid reductases to convert steroid hormones into the 3-alpha/5-alpha and 3-alpha/5-beta-tetrahydrosteroids. Catalyzes the inactivation of the most potent androgen 5-alpha-dihydrotestosterone (5-alpha- DHT) to 5-alpha-androstane-3-alpha,17-beta-diol (3-alpha-diol). Has a high bile-binding ability.
Qin K.-N.,et al.J. Steroid Biochem. Mol. Biol. 46:673-679(1993).
Ciaccio P.J.,et al.Biochim. Biophys. Acta 1186:129-132(1994).
Qin K.-N.,et al.Gene 149:357-361(1994).
Dufort I.,et al.Biochem. Biophys. Res. Commun. 228:474-479(1996).
Shiraishi H.,et al.Biochem. J. 334:399-405(1998).
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