Human Sacsin (SACS) activation kit by CRISPRa

CAT#: GA108840

SACS CRISPRa kit - CRISPR gene activation of human sacsin molecular chaperone



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (2)
SACS Antibody - C-terminal region
    • 100 ul

CNY 5,250.00


SACS (Myc-DDK-tagged)-Human spastic ataxia of Charlevoix-Saguenay (sacsin) (SACS)
    • 10 ug

CNY 43,688.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol SACS
Locus ID 26278
Kit Components

GA108840G1, Sacsin gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA108840G2, Sacsin gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA108840G3, Sacsin 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_001278055, NM_014363
Synonyms ARSACS; DNAJC29; SPAX6
Summary This gene encodes the sacsin protein, which includes a UbL domain at the N-terminus, a DnaJ domain, and a HEPN domain at the C-terminus. The gene is highly expressed in the central nervous system, also found in skin, skeletal muscles and at low levels in the pancreas. This gene includes a very large exon spanning more than 12.8 kb. Mutations in this gene result in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity and peripheral neuropathy. The authors of a publication on the effects of siRNA-mediated sacsin knockdown concluded that sacsin protects against mutant ataxin-1 and suggest that "the large multi-domain sacsin protein is able to recruit Hsp70 chaperone action and has the potential to regulate the effects of other ataxia proteins" (Parfitt et al., PubMed: 19208651). A pseudogene associated with this gene is located on chromosome 11. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 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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