Human RRBP1 activation kit by CRISPRa

CAT#: GA104228

RRBP1 CRISPRa kit - CRISPR gene activation of human ribosome binding protein 1



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
RRBP1 mouse monoclonal antibody,clone OTI3F1
    • 100 ul

CNY 1,999.00
CNY 2,700.00


RRBP1 (Myc-DDK-tagged)-Human ribosome binding protein 1 homolog 180kDa (dog) (RRBP1), transcript variant 1
    • 10 ug

CNY 10,728.00


RRBP1 mouse monoclonal antibody,clone OTI3F1
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol RRBP1
Locus ID 6238
Kit Components

GA104228G1, RRBP1 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA104228G2, RRBP1 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA104228G3, RRBP1 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_001042576, NM_004587, NM_001365613
Synonyms ES/130; ES130; hES; RRp
Summary This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12. [provided by RefSeq, Apr 2012]
*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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