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Vitamin D Receptor (VDR) (NM_001017535) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC219628L1V
- LentiORF®
-
Lenti ORF particles, VDR (Myc-DDK tagged) - Human vitamin D (1,25- dihydroxyvitamin D3) receptor (VDR), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 8,930.00
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规格
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Specifications
| Product Data | |
| Product Name | Vitamin D Receptor (VDR) (NM_001017535) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | NR1I1; PPP1R163 |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_001017535 |
| ORF Size | 1281 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC219628).
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| 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_001017535.1 |
| RefSeq Size | 4791 bp |
| RefSeq ORF | 1284 bp |
| Locus ID | 7421 |
| Protein Families | Druggable Genome, Nuclear Hormone Receptor, Transcription Factors |
| MW | 48.1 kDa |
| Gene Summary | This gene encodes vitamin D3 receptor, which is a member of the nuclear hormone receptor superfamily of ligand-inducible transcription factors. This receptor also functions as a receptor for the secondary bile acid, lithocholic acid. Downstream targets of vitamin D3 receptor are principally involved in mineral metabolism, though this receptor regulates a variety of other metabolic pathways, such as those involved in immune response and cancer. Mutations in this gene are associated with type II vitamin D-resistant rickets. A single nucleotide polymorphism in the initiation codon results in an alternate translation start site three codons downstream. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Jun 2018] |
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