CYP21A2 (NM_001128590) Human 3' UTR Clone

Specifications

Product Data
Product Name	CYP21A2 (NM_001128590) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CA21H; CAH1; CPS1; CYP21; CYP21B; P450c21B
ACCN	NM_001128590
Insert Size	538 bp
Sequence Data	Insert Sequence (showhide) >SC206853 3’UTR clone of NM_001128590 The sequence shown below is from the reference sequence of NM_001128590. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGGGCCCACAGCCCGGGCCAGAGCCAGTGATGGGGCAGGACCGATGCCAGCCGGGTACCTCAGTTTCTC CTTTATTGCTCCCGTACGAACCCCTCCCCTCCCCCCTGTAAACACAGTGCTGCGAGATCGCTGGCAGAG AAGGCTTCCTCCAGCGGCTGGGTGGTGAAGGACCCTGGCTCTTCTCTCGGGGCGACCCCTCAGTGCTCG GCAGTCATACTGGGGTGCGAGAGAGGTGGGCAGCAGCTCAGCCTCCCCCCGCTGGGGAGCGAAAGTTTC TTGGTCTCAGCTTCATTTCCGTGAAGGGCACCGAGAACTCGAAGCCCTTCCAGTGGTACCAGCTCACTC CCTGGGAAAGGGGTTGTCAAGAGAGAGTCAAAGCCGGATGTCCCATCTGCTCTTCCCGTTCCCCTTAAG GAGGTAGCTCCCAGCACTCAACCAACCTCCCCGCAGAGCTCCCTTCCTGACCCTCCGCTGCAGAGGATT GAGGCTTAATTCTGAGCTGGCCCTTTCCAGCCAATAAATCAACTCCAGCTCCCTC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_001128590.4
Synonyms	CA21H; CAH1; CPS1; CYP21; CYP21B; P450c21B
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, Jul 2008]
Locus ID	1589
MW	18.7

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