NCF2 (NM_001127651) Human 3' UTR Clone

Specifications

Product Data
Product Name	NCF2 (NM_001127651) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	NCF-2; NOXA2; P67-PHOX; P67PHOX
ACCN	NM_001127651
Insert Size	586 bp
Sequence Data	Insert Sequence (showhide) >SC207628 3’UTR clone of NM_001127651 The sequence shown below is from the reference sequence of NM_001127651. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GATTTGGAAAGCACTCGGAGAGAAGTCTAGGATGTTTCACAAACTACAAAGCTGAAGAAAATGAAGCCC TATTACTTGTTTGTAAGATTTAGCACCCTTCTGCTGTATACTGTACTGAGACATTACAGTTTGGAAGTG TTAACTATTTATTCCCTGTTAAAATTTAACCTACTAGACAATGATGTGAGTACCCAGGATGATTTCCTG GGGCACAGTGGGTGAGGAGATGGGGACAGGTGAATGGAGGAGTTAGGGGAGAGGAAAAGTGGATGGAAG TGTCTGGAAAGGGCACGAGAGAGTCTTCCAGGTACTGATCCTGTTTCTTGCTCTGAGTGCTAGCTAGCC AGCTGTGTTCACACTGTAAACATTCATCAAGCTGTACATTTGGTGCACTTTTCTGTGTCATACCACAAT AAAAAAAAACCTAGCATCTTACAAAAACAAGACACCCAAGTCCAGGCCCAAGGAGTAAGTACAAATATT CCTGTTTCTGAACCATTACTGTAATTGGCTCTTAAGGCTTGAAGTAACCTTATAGGTTACTCATAAGGC ATATACAAATAAACTTGTTTGTTTTCTTTTTTCA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_001127651.3
Synonyms	NCF-2; NOXA2; P67-PHOX; P67PHOX
Summary	This gene encodes neutrophil cytosolic factor 2, the 67-kilodalton cytosolic subunit of the multi-protein NADPH oxidase complex found in neutrophils. This oxidase produces a burst of superoxide which is delivered to the lumen of the neutrophil phagosome. Mutations in this gene, as well as in other NADPH oxidase subunits, can result in chronic granulomatous disease, a disease that causes recurrent infections by catalase-positive organisms. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2010]
Locus ID	4688
MW	22.1

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