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CYP21A2 (NM_000500) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC216416L1V
- LentiORF®
-
Lenti ORF particles, CYP21A2 (Myc-DDK tagged) - Human cytochrome P450, family 21, subfamily A, polypeptide 2 (CYP21A2), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
| Product Data | |
| Product Name | CYP21A2 (NM_000500) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CA21H; CAH1; CPS1; CYP21; CYP21B; P450c21B |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_000500 |
| ORF Size | 1485 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC216416).
|
| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_000500.5 |
| RefSeq Size | 2131 bp |
| RefSeq ORF | 1488 bp |
| Locus ID | 1589 |
| Domains | p450 |
| Protein Families | Druggable Genome, P450 |
| Protein Pathways | C21-Steroid hormone metabolism, Metabolic pathways |
| MW | 56 kDa |
| 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, Jul 2008] |
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