Human GNB1L activation kit by CRISPRa

CAT#: GA110190

GNB1L CRISPRa kit - CRISPR gene activation of human G protein subunit beta 1 like



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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 Anti-GNB1L Antibody
    • 100 ul

CNY 5,250.00


GNB1L (Myc-DDK-tagged)-Human guanine nucleotide binding protein (G protein), beta polypeptide 1-like (GNB1L)
    • 10 ug

CNY 2,400.00
CNY 3,990.00


GNB1L Rabbit polyclonal Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol GNB1L
Locus ID 54584
Kit Components

GA110190G1, GNB1L gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA110190G2, GNB1L gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA110190G3, GNB1L 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_022446, NM_053004
Synonyms DGCRK3; FKSG1; GY2; WDR14; WDVCF
Summary This gene encodes a G-protein beta-subunit-like polypeptide which is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene. [provided by RefSeq, Jul 2008]
*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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