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SNTG1 (NM_018967) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC211170L4V
- LentiORF®
-
Lenti ORF particles, SNTG1 (mGFP-tagged) - Human syntrophin, gamma 1 (SNTG1), 200ul, >10^7 TU/mL
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CNY 9,975.00
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Specifications
| Product Data | |
| Product Name | SNTG1 (NM_018967) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | G1SYN; SYN4 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_018967 |
| ORF Size | 1551 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC211170).
|
| 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_018967.2, NP_061840.1 |
| RefSeq Size | 3398 bp |
| RefSeq ORF | 1554 bp |
| Locus ID | 54212 |
| Domains | PDZ, PH |
| MW | 58 kDa |
| Gene Summary | The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016] |
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