Human PTPN20B (PTPN20) activation kit by CRISPRa

Specifications

Product Data
Format	3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol	PTPN20
Locus ID	26095
Kit Components	GA108749G1, PTPN20B gRNA vector 1 in pCas-Guide-GFP-CRISPRa GA108749G2, PTPN20B gRNA vector 2 in pCas-Guide-GFP-CRISPRa GA108749G3, PTPN20B 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_001042357, NM_001042358, NM_001042359, NM_001042360, NM_001042361, NM_001042362, NM_001042363, NM_001042364, NM_001042365, NM_001320681, NM_001320682, NM_001320683, NM_001320684, NM_001320685, NM_001320686, NM_001320688, NM_001320689, NM_001320690, NM_001320691, NM_015605, NM_001352521, NM_001352522, NM_001352523, NM_001352524, NM_001352525, NM_001352526, NM_001352527, NM_001352528, NM_001352529, NM_001352530, NM_001352531, NM_001352532, NM_001352533, NM_001352534, NM_001352535, NM_001352536, NM_001352537, NM_001352538, NM_001352539, NM_001352540, NM_001352541, NM_001352542, NM_001352543, NM_001352544, NM_001352545, NM_001352546, NM_001352547, NM_001352548, NM_001352549, NM_001352550, NM_001352551, NM_001352552, NM_001352553, NM_001352554, NM_001352555, NR_148022, NR_148023, NR_148024
Synonyms	bA42B19.1; bA142I17.1; CT126; PTPN20A; PTPN20B
Summary	The product of this gene belongs to the family of classical tyrosine-specific protein tyrosine phosphatases. Many protein tyrosine phosphatases have been shown to regulate fundamental cellular processes. The encoded protein appears to be targeted to sites of actin polymerization. A pseudogene of this gene has been defined on chromosome 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]

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