TACI (TNFRSF13B) (NM_012452) Human 3' UTR Clone

Specifications

Product Data
Product Name	TACI (TNFRSF13B) (NM_012452) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CD267; CVID; CVID2; IGAD2; RYZN; TACI; TNFRSF14B
ACCN	NM_012452
Insert Size	496 bp
Sequence Data	Insert Sequence (showhide) >SC206510 3’UTR clone of NM_012452 The sequence shown below is from the reference sequence of NM_012452. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCTGCCCAGGAGGGGGGCCCAGGTGCATAAATGGGGGTCAGGGAGGGAAAGGAGGAGGGAGAGAGATGG AGAGGAGGGGAGAGAGAAAGAGAGGTGGGGAGAGGGGAGAGAGATATGAGGAGAGAGAGACAGAGGAGG CAGAGAGGGAGAGAAACAGAGGAGACAGAGAGGGAGAGAGAGACAGAGGGAGAGAGAGACAGAGGGGAA GAGAGGCAGAGAGGGAAAGAGGCAGAGAAGGAAAGAGACAGGCAGAGAAGGAGAGAGGCAGAGAGGGAG AGAGGCAGAGAGGGAGAGAGGCAGAGAGACAGAGAGGGAGAGAGGGACAGAGAGAGATAGAGCAGGAGG TCGGGGCACTCTGAGTCCCAGTTCCCAGTGCAGCTGTAGGTCGTCATCACCTAACCACACGTGCAATAA AGTCCTCGTGCCTGCTGCTCACAGCCCCCGAGAGCCCCTCCTCCTGGAGAATAAAACCTTTGGCAGCTG CCCTTCCTCACTG 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_012452.3
Synonyms	CD267; CVID; CVID2; IGAD2; RYZN; TACI; TNFRSF14B
Summary	The protein encoded by this gene is a lymphocyte-specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein induces activation of the transcription factors NFAT, AP1, and NF-kappa-B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Locus ID	23495
MW	19.6

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