TBX1 (NM_005992) Human 3' UTR Clone
CAT#: SC203754
3' UTR clone of T-box 1 (TBX1) transcript variant B for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | TBX1 (NM_005992) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CAFS; CATCH22; CTHM; DGCR; DGS; DORV; TBX1C; TGA; VCF; VCFS |
ACCN | NM_005992 |
Insert Size | 320 bp |
Sequence Data |
>SC203754 3’UTR clone of NM_005992
The sequence shown below is from the reference sequence of NM_005992. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGAGACCACCACACTGCAAGGACACTTGAAGGTACTCAGGTTTCAGAGCCCAAGTCAGGAGGTCAAGT GTGCATGCAAGAGGTGGCAGGGGACAGATGTGCTGCTGTTCCCAGGCCACCTGCACAGCTGGATGGTGG AAGCAGTTCACTTAAAGGCCATGAGTTACTCGGGAGGCTGAGGCAGGAGGATCACTTGAGCCTATTAGT TGGAGGCTGCAGTAAGCTATGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACCCCCACTG TCCCTGGTCTCTTAAAAGAAAAAACAAACAAACAAACCAAAAAA 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_005992.1 |
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 |
MW | 11.9 |
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