Human CHRNA2 activation kit by CRISPRa

CAT#: GA100812

CHRNA2 CRISPRa kit - CRISPR gene activation of human cholinergic receptor nicotinic alpha 2 subunit



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (2)
Rabbit Polyclonal Anti-CHRNA2 Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


CHRNA2 (Myc-DDK-tagged)-Human cholinergic receptor, nicotinic, alpha 2 (neuronal) (CHRNA2)
    • 10 ug

CNY 3,936.00
CNY 3,990.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol CHRNA2
Locus ID 1135
Kit Components

GA100812G1, CHRNA2 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA100812G2, CHRNA2 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA100812G3, CHRNA2 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_000742, NM_001282455, NM_001347705, NM_001347706, NM_001347707, NM_001347708
Synonyms cholinergic receptor, nicotinic, alpha 2 (neuronal); cholinergic receptor, nicotinic, alpha polypeptide 2 (neuronal); OTTHUMP00000128276
Summary Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels formed by a pentameric arrangement of alpha and beta subunits to create distinct muscle and neuronal receptors. Neuronal receptors are found throughout the peripheral and central nervous system where they are involved in fast synaptic transmission. This gene encodes an alpha subunit that is widely expressed in the brain. The proposed structure for nAChR subunits is a conserved N-terminal extracellular domain followed by three conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region. Mutations in this gene cause autosomal dominant nocturnal frontal lobe epilepsy type 4. Single nucleotide polymorphisms (SNPs) in this gene have been associated with nicotine dependence. [provided by RefSeq, Nov 2009]
*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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