Human SLC26A4 activation kit by CRISPRa

Specifications

Product Data
Format	3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol	SLC26A4
Locus ID	5172
Kit Components	GA103468G1, SLC26A4 gRNA vector 1 in pCas-Guide-GFP-CRISPRa GA103468G2, SLC26A4 gRNA vector 2 in pCas-Guide-GFP-CRISPRa GA103468G3, SLC26A4 gRNA vector 3 in pCas-Guide-GFP-CRISPRa 1 CRISPRa-Enhancer vector, SKU GE100056 1 CRISPRa scramble vector, SKU GE100077
Reference Data
RefSeq	NM_000441
Synonyms	DFNB4; EVA; PDS; TDH2B
Summary	Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008]

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