Mouse Dmd activation kit by CRISPRa
CAT#: GA201093
Dmd CRISPRa kit - CRISPR gene activation of mouse dystrophin, muscular dystrophy
CNY 12,255.00
货期*
4周
规格
Specifications
Product Data | |
Format | 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug) |
Symbol | Dmd |
Locus ID | 13405 |
Kit Components | GA201093G1, Dmd gRNA vector 1 in pCas-Guide-GFP-CRISPRa GA201093G2, Dmd gRNA vector 2 in pCas-Guide-GFP-CRISPRa GA201093G3, Dmd 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 | |
Synonyms | Dp71; Dp427; DXSmh7; DXSmh9; dys; mdx; pke |
Summary | This gene encodes a large, rod-like cytoskeletal protein which is found at the inner surface of muscle fibers in skeletal and cardiac muscles. The encoded protein, dystrophin, is part of the dystrophin-glycoprotein complex, which bridges the inner cytoskeleton (F-actin) and the extra-cellular matrix. This protein is required for proper development and organization of myofibers as contractile units in striated muscles. Mutations in the human gene cause Duchenne and Becker Muscular Dystrophies and a form of heart disease called DMD-associated dilated cardiomyopathy. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Sep 2015] |
Documents
Resources
基因表达相关资源 |
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