Human KIDINS220 activation kit by CRISPRa

Specifications

Product Data
Format	3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol	KIDINS220
Locus ID	57498
Kit Components	GA111539G1, KIDINS220 gRNA vector 1 in pCas-Guide-GFP-CRISPRa GA111539G2, KIDINS220 gRNA vector 2 in pCas-Guide-GFP-CRISPRa GA111539G3, KIDINS220 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_020738, NM_001348729, NM_001348731, NM_001348732, NM_001348734, NM_001348735, NM_001348736, NM_001348738, NM_001348739, NM_001348740, NM_001348741, NM_001348742, NM_001348743, NM_001348745, NR_145964, NR_145965
Synonyms	ARMS
Summary	This gene encodes a transmembrane protein that is preferentially expressed in the nervous system where it controls neuronal cell survival, differentiation into exons and dendrites, and synaptic plasticity. The encoded protein interacts with membrane receptors, cytosolic signaling components, and cytoskeletal proteins, serving as a scaffold that mediates crosstalk between the neurotrophin pathway and several other intracellular signaling pathways. Aberrant expression of this gene is associated with the onset of various neuropsychiatric disorders and neurodegenerative diseases, including Alzheimer's disease. Naturally occurring mutations in this gene are associated with a syndrome characterized by spastic paraplegia, intellectual disability, nystagmus and obesity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]

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