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Syntrophin alpha 1 (SNTA1) (NM_003098) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC204480L3V
- LentiORF®
-
Lenti ORF particles, SNTA1 (Myc-DDK tagged) - Human syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component) (SNTA1), 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
| Product Data | |
| Product Name | Syntrophin alpha 1 (SNTA1) (NM_003098) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | dJ1187J4.5; LQT12; SNT1; TACIP1 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_003098 |
| ORF Size | 1515 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC204480).
|
| 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_003098.2 |
| RefSeq Size | 2345 bp |
| RefSeq ORF | 1518 bp |
| Locus ID | 6640 |
| Domains | PDZ, PH |
| MW | 53.9 kDa |
| Gene Summary | Syntrophins are cytoplasmic peripheral membrane scaffold proteins that are components of the dystrophin-associated protein complex. This gene is a member of the syntrophin gene family and encodes the most common syntrophin isoform found in cardiac tissues. The N-terminal PDZ domain of this syntrophin protein interacts with the C-terminus of the pore-forming alpha subunit (SCN5A) of the cardiac sodium channel Nav1.5. This protein also associates cardiac sodium channels with the nitric oxide synthase-PMCA4b (plasma membrane Ca-ATPase subtype 4b) complex in cardiomyocytes. This gene is a susceptibility locus for Long-QT syndrome (LQT) - an inherited disorder associated with sudden cardiac death from arrhythmia - and sudden infant death syndrome (SIDS). This protein also associates with dystrophin and dystrophin-related proteins at the neuromuscular junction and alters intracellular calcium ion levels in muscle tissue. [provided by RefSeq, Jan 2013] |
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