Human FGD4 activation kit by CRISPRa

CAT#: GA114753

FGD4 CRISPRa kit - CRISPR gene activation of human FYVE, RhoGEF and PH domain containing 4



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
Rabbit polyclonal antibody to FGD4 (FYVE, RhoGEF and PH domain containing 4)
    • 100 ul

CNY 6,281.00


FGD4 (Myc-DDK-tagged)-Human FYVE, RhoGEF and PH domain containing 4 (FGD4)
    • 10 ug

CNY 5,608.00
CNY 5,800.00


Rabbit Polyclonal FGD4 Antibody
    • 100 ug

CNY 5,302.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol FGD4
Locus ID 121512
Kit Components

GA114753G1, FGD4 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA114753G2, FGD4 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA114753G3, FGD4 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_001304480, NM_001304481, NM_001304483, NM_001304484, NM_001330373, NM_001330374, NM_139241, NM_001370297, NM_001370298
Synonyms CMT4H; FRABP; ZFYVE6
Summary This gene encodes a protein that is involved in the regulation of the actin cytoskeleton and cell shape. This protein contains an actin filament-binding domain, which together with its Dbl homology domain and one of its pleckstrin homology domains, can form microspikes. This protein can activate MAPK8 independently of the actin filament-binding domain, and it is also involved in the activation of CDC42 via the exchange of bound GDP for free GTP. The activation of CDC42 also enables this protein to play a role in mediating the cellular invasion of Cryptosporidium parvum, an intracellular parasite that infects the gastrointestinal tract. Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H), a disorder of the peripheral nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 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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