Human SEMA4A activation kit by CRISPRa
CAT#: GA112016
SEMA4A CRISPRa kit - CRISPR gene activation of human semaphorin 4A
CNY 12255.00
Specifications
| Product Data | |
| Format | 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug) |
| Symbol | SEMA4A |
| Locus ID | 64218 |
| Kit Components | GA112016G1, SEMA4A gRNA vector 1 in pCas-Guide-GFP-CRISPRa GA112016G2, SEMA4A gRNA vector 2 in pCas-Guide-GFP-CRISPRa GA112016G3, SEMA4A gRNA vector 3 in pCas-Guide-GFP-CRISPRa 1 CRISPRa-Enhancer vector, SKU GE100056 1 CRISPRa scramble vector, SKU GE100077 |
| Reference Data | |
| RefSeq | NM_001193300, NM_001193301, NM_001193302, NM_022367, NM_001370567, NM_001370569, NM_001370571, NM_001370568 |
| Synonyms | CORD10; RP35; SEMAB; SEMB |
| Summary | This gene encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single-pass type I membrane protein containing an immunoglobulin-like C2-type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons. It is an activator of T-cell-mediated immunity and suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration and proliferation in vitro and angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010] |
Documents
Resources
| 基因表达相关资源 |
Other Versions
| SKU | Description | Size | Price |
|---|---|---|---|
| KN402231 | SEMA4A - KN2.0, Human gene knockout kit via CRISPR, non-homology mediated. |
CNY 8680.00 |
