Human Hairless (HR) activation kit by CRISPRa

CAT#: GA110985

HR CRISPRa kit - CRISPR gene activation of human HR lysine demethylase and nuclear receptor corepressor



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
HR mouse monoclonal antibody, clone OTI1D9 (formerly 1D9)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


HR (Myc-DDK-tagged)-Human hairless homolog (mouse) (HR), transcript variant 1
    • 10 ug

CNY 8,280.00


HR mouse monoclonal antibody, clone OTI1D9 (formerly 1D9)
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol HR
Locus ID 55806
Kit Components

GA110985G1, Hairless gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA110985G2, Hairless gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA110985G3, Hairless 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_005144, NM_018411
Synonyms ALUNC; AU; HSA277165; HYPT4; MUHH; MUHH1
Summary This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by a regulatory open reading frame (ORF) that exists upstream of the primary ORF. Mutations in this upstream ORF cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]
*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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