TBX1 (NM_080647) Human 3' UTR Clone

Specifications

Product Data
Product Name	TBX1 (NM_080647) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CAFS; CATCH22; CTHM; DGCR; DGS; DORV; TBX1C; TGA; VCF; VCFS
ACCN	NM_080647
Insert Size	491 bp
Sequence Data	Insert Sequence (showhide) >SC206272 3' UTR clone of NM_080647 The sequence shown below is from the reference sequence of NM_080647. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GCTCCTACGACTATTGCCCCAGATAACACGGGCCCTGTCGCGCTCCCGCCCCGGTCCTGCACAGCCCCGA AGTTCGCCGGGCCCGGCCACCCTGCCCCAAGGGCAAGCAAGGAATACGTTCCCCCAGCCCCAGGGGCCAC CGCGGCTCTCCCCTTCCCCAGCCTCGAAGCCATGGGGGCCCCCTCGCCACCCCCAGCCCCTTGGGCTATC GAAGTATCCGGTTCCCCAGTCCCTGGAGCCACCGCGGGTCCTTCCCCGGCCCCGAGGGCCAAGGGGGTCC CCGCCCGCCAGTGCCAAAGCGCCCGGTCGGAGGCGGAAGGAAGTGATATTTATTGTTCTCCCCGAGACCG CGTCGCCCGCGGCCCGGCCGGCAGTTGCAGTGTAGACAGCCCGAGAGCCCCGCCTGCAGGCGGTGTAGAT ACATGTAGATACTGTAGATACTGTAGATACCGCCCCGGCGCCGACTTGATAAACGGTTTCGCCTCTTTTG G ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_080647.1
Synonyms	CAFS; CATCH22; CTHM; DGCR; DGS; DORV; TBX1C; TGA; VCF; VCFS
Summary	This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98% amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Locus ID	6899

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