Human Fukutin (FKTN) activation kit by CRISPRa

CAT#: GA101554

FKTN CRISPRa kit - CRISPR gene activation of human fukutin

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Find the corresponding CRISPRi Inhibitor Kit

USD 1,290.00

2 Weeks*

Size
    • 1 kit

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Frequently bought together (1)
Rabbit Polyclonal antibody to Fukutin (fukutin)
    • 100 ul

USD 415.00

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Specifications

Product Data
Format 3gRNAs, 1 scramble ctrl and 1 enhancer vector
Symbol FKTN
Locus ID 2218
Kit Components

GA101554G1, Fukutin gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA101554G2, Fukutin gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA101554G3, Fukutin gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Disclaimer The kit is designed based on the best knowledge of CRISPa 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_001079802, NM_001198963, NM_006731, NM_001351496, NM_001351497, NM_001351498, NM_001351499, NM_001351500, NM_001351501, NM_001351502, NR_147213, NR_147214
Synonyms CMD1X; FCMD; LGMD2M; MDDGA4; MDDGB4; MDDGC4
Summary 'The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2010]'

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*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.