Human Synapsin I (SYN1) activation kit by CRISPRa

CAT#: GA104715

SYN1 CRISPRa kit - CRISPR gene activation of human synapsin I



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
Rabbit Polyclonal Anti-SYN1 Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


SYN1 (Myc-DDK-tagged)-Human synapsin I (SYN1), transcript variant Ib
    • 10 ug

CNY 4,904.00
CNY 5,800.00


Phospho-Synapsin I (Ser9) Rabbit polyclonal Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol SYN1
Locus ID 6853
Kit Components

GA104715G1, Synapsin I gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA104715G2, Synapsin I gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA104715G3, Synapsin I 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_006950, NM_133499
Synonyms SYN1a; SYN1b; SYNI
Summary This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis. The protein encoded serves as a substrate for several different protein kinases and phosphorylation may function in the regulation of this protein in the nerve terminal. Mutations in this gene may be associated with X-linked disorders with primary neuronal degeneration such as Rett syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
*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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