Search
Search
Invitrogen
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoTitle}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
Peptide Sequence: RLQGTGVTTY AVHPGVVRSE LVRHSSLLCL LWRLFSPFVK TAREGAQTSL HCALAEGLEP LSGKYFSDCK RTWVSPRARN NKTAERLWNV SCELLGIRWE
The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: All-trans and 9-cis retinol dehydrogenase; LCA3; Retinol dehydrogenase 12; retinol dehydrogenase 12, all-trans and 9-cis; Short chain dehydrogenase/reductase family 7C member 2; short chain dehydrogenase/reductase family 7C, member 2
基因别名: LCA13; RDH12; RP53; SDR7C2
UniProt ID: (Human) Q96NR8
Entrez Gene ID: (Human) 145226