Human SHANK3 activation kit by CRISPRa
CAT#: GA113856
SHANK3 CRISPRa kit - CRISPR gene activation of human SH3 and multiple ankyrin repeat domains 3
CNY 12,255.00
Specifications
Product Data | |
Format | 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug) |
Symbol | SHANK3 |
Locus ID | 85358 |
Kit Components | GA113856G1, SHANK3 gRNA vector 1 in pCas-Guide-GFP-CRISPRa GA113856G2, SHANK3 gRNA vector 2 in pCas-Guide-GFP-CRISPRa GA113856G3, SHANK3 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_001080420, NM_033517 |
Synonyms | DEL22q13.3; KIAA1650; PROSAP2; PSAP2; SPANK-2 |
Summary | This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012] |
Documents
Resources
基因表达相关资源 |
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