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CYP21A2 Pre-design Chimera RNAi

  • Catalog # : H00001589-R01
  • Visit Frequency :
  • Countries :
  • Specification
  • Product Description:
  • Homo sapiens cytochrome P450, family 21, subfamily A, polypeptide 2 (CYP21A2), mRNA.
  • Reactivity:
  • Human
  • Supplied Product:
  • DEPC water
  • Target Refseq:
  • NM_000500
  • Storage Instruction:
  • Store at -20°C, do not exceed 4 - 5 freeze-thaw cycles to ensure product integrity.
  • Note:
  • Position of the Chimera RNAi.

  • Publication Reference
  • Applications
  • RNAi Knockdown
  • Application Image
  • RNAi Knockdown
  • Gene Information
  • Entrez GeneID:
  • 1589
  • Gene Name:
  • CYP21A2
  • Gene Alias:
  • CA21H,CAH1,CPS1,CYP21,CYP21B,MGC150536,MGC150537,P450c21B
  • Gene Description:
  • cytochrome P450, family 21, subfamily A, polypeptide 2
  • Gene Summary:
  • This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and hydroxylates steroids at the 21 position. Its activity is required for the synthesis of steroid hormones including cortisol and aldosterone. Mutations in this gene cause congenital adrenal hyperplasia. A related pseudogene is located near this gene; gene conversion events involving the functional gene and the pseudogene are thought to account for many cases of steroid 21-hydroxylase deficiency. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • 21-hydroxylase,OTTHUMP00000062684,cytochrome P450, family 21, subfamily A, polypepide 2,cytochrome P450, subfamily XXIA (steroid 21-hydroxylase, congenital adrenal hyperplasia), polypeptide 2,dJ34F7.3 (cytochrome P450, subfamily XXIA (steroid 21-hydroxyla
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