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GPR172A (SLC52A2) (NM_024531) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC202512L4V
- LentiORF®
-
Lenti ORF particles, SLC52A2 (mGFP-tagged) - Human G protein-coupled receptor 172A (GPR172A), 200ul, >10^7 TU/mL
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CNY 9,975.00
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Specifications
| Product Data | |
| Product Name | GPR172A (SLC52A2) (NM_024531) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BVVLS2; D15Ertd747e; GPCR41; GPR172A; hRFT3; PAR1; RFT3; RFVT2 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_024531 |
| ORF Size | 1335 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC202512).
|
| 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_024531.3 |
| RefSeq Size | 1900 bp |
| RefSeq ORF | 1338 bp |
| Locus ID | 79581 |
| Protein Families | Druggable Genome, GPCR, Transmembrane |
| MW | 45.8 kDa |
| Gene Summary | This gene encodes a membrane protein which belongs to the riboflavin transporter family. In humans, riboflavin must be obtained by intestinal absorption because it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed to the coenzymes flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which then act as intermediaries in many cellular metabolic reactions. Paralogous members of the riboflavin transporter gene family are located on chromosomes 17 and 20. Unlike other members of this family, this gene has higher expression in brain tissue than small intestine. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2 - an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunction, and axial and limb hypotonia. [provided by RefSeq, Jul 2012] |
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