Human Syntrophin alpha 1 (SNTA1) activation kit by CRISPRa

CAT#: GA104551

SNTA1 CRISPRa kit - CRISPR gene activation of human syntrophin alpha 1



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
SNTA1 (Syntrophin alpha 1) mouse monoclonal antibody, clone OTI1H10 (formerly 1H10)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


SNTA1 (Myc-DDK-tagged)-Human syntrophin, alpha 1 (dystrophin-associated protein A1, 59kDa, acidic component) (SNTA1)
    • 10 ug

CNY 3,760.00
CNY 4,560.00


SNTA1 (Syntrophin alpha 1) mouse monoclonal antibody, clone OTI2B4 (formerly 2B4)
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol SNTA1
Locus ID 6640
Kit Components

GA104551G1, Syntrophin alpha 1 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA104551G2, Syntrophin alpha 1 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA104551G3, Syntrophin alpha 1 gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Disclaimer These products are manufactured and supplied by OriGene under license from ERS. The kit is designed based on the best knowledge of CRISPRa SAM technology. The efficiency of the activation can be affected by many factors, including nucleosome occupancy status, chromatin structure and the gene expression level of the target, etc.
Reference Data
RefSeq NM_003098
Synonyms dJ1187J4.5; LQT12; SNT1; TACIP1
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]
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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