Human NYREN18 (NUB1) activation kit by CRISPRa

CAT#: GA109934

NUB1 CRISPRa kit - CRISPR gene activation of human negative regulator of ubiquitin like proteins 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)
NUB1 (NYREN18) mouse monoclonal antibody, clone OTI4H2 (formerly 4H2)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


NUB1 (Myc-DDK-tagged)-Human negative regulator of ubiquitin-like proteins 1 (NUB1)
    • 10 ug

CNY 4,472.00
CNY 4,560.00


NUB1 (NYREN18) mouse monoclonal antibody, clone OTI1B7 (formerly 1B7)
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol NUB1
Locus ID 51667
Kit Components

GA109934G1, NYREN18 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA109934G2, NYREN18 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA109934G3, NYREN18 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_001243351, NM_016118, NM_001363529
Synonyms BS4; NUB1L; NYREN18
Summary This gene encodes a protein that functions as a negative regulator of NEDD8, a ubiquitin-like protein that conjugates with cullin family members in order to regulate vital biological events. The protein encoded by this gene regulates the NEDD8 conjugation system post-transcriptionally by recruiting NEDD8 and its conjugates to the proteasome for degradation. This protein interacts with the product of the AIPL1 gene, which is associated with Leber congenital amaurosis, an inherited retinopathy, and mutations in that gene can abolish interaction with this protein, which may contribute to the pathogenesis. This protein is also known to accumulate in Lewy bodies in Parkinson's disease and dementia with Lewy bodies, and in glial cytoplasmic inclusions in multiple system atrophy, with this abnormal accumulation being specific to alpha-synucleinopathy lesions. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]
*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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