Human NOTCH1 activation kit by CRISPRa

CAT#: GA103238

NOTCH1 CRISPRa kit - CRISPR gene activation of human notch receptor 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)
Anti-Notch1 mouse monoclonal antibody, clone OTI3E12 (formerly 3E12)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


NOTCH1 (Myc-DDK-tagged)-Human notch 1 (NOTCH1)
    • 10 ug

CNY 25,312.00


NOTCH1 mouse monoclonal antibody, clone OTI2E7 (formerly 2E7)
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol NOTCH1
Locus ID 4851
Kit Components

GA103238G1, NOTCH1 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA103238G2, NOTCH1 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA103238G3, NOTCH1 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_017617
Synonyms AOS5; AOVD1; hN1; TAN1
Summary This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymphocytic leukemia, and head and neck squamous cell carcinoma. [provided by RefSeq, Jan 2016]
*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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