Human QPRT activation kit by CRISPRa

CAT#: GA108332

QPRT CRISPRa kit - CRISPR gene activation of human quinolinate phosphoribosyltransferase



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
QPRT mouse monoclonal antibody, clone OTI1C10 (formerly 1C10)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


QPRT (Myc-DDK-tagged)-Human quinolinate phosphoribosyltransferase (QPRT)
    • 10 ug

CNY 3,600.00


QPRT mouse monoclonal antibody, clone OTI7A8 (formerly 7A8)
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol QPRT
Locus ID 23475
Kit Components

GA108332G1, QPRT gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA108332G2, QPRT gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA108332G3, QPRT 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_001318249, NM_001318250, NM_014298, NR_134536
Synonyms HEL-S-90n; QPRTase
Summary This gene encodes a key enzyme in catabolism of quinolinate, an intermediate in the tryptophan-nicotinamide adenine dinucleotide pathway. Quinolinate acts as a most potent endogenous exitotoxin to neurons. Elevation of quinolinate levels in the brain has been linked to the pathogenesis of neurodegenerative disorders such as epilepsy, Alzheimer's disease, and Huntington's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
*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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