DACH2 (NM_053281) Human 3' UTR Clone

Specifications

Product Data
Product Name	DACH2 (NM_053281) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_053281
Insert Size	477 bp
Sequence Data	Insert Sequence (showhide) >SC206030 3’UTR clone of NM_053281 The sequence shown below is from the reference sequence of NM_053281. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAAATGGCACAACAGTTGTATTCAGCCTGAAAGGTCCTCGCTGGCTTTACATAAATGAAGATGCTTGTG ATTCCAGTTTATCTCTGAAACTATTCAACATGGAGTTATTTCAGTTTTGTTTATCAGCAAAGCTTTGTT TACTGAAGGAGCTATTTAATCTATGTTACATTAAAAAAGAAACGCGTGTACATTTTAAAAGCAATGATG TAAACTTTGTTCTTGCATTAGACTGACCAGTTTAAAAATATGAACTAAAACCTAATGGCTAAAGTAACT TGACCATATTTGATGCTTTTCTATGCTCATTTCAACTTGGCTTTTTGTCTTTTAAATTTTTAAAAAATG CAGTAGTGTGTTAGAGACTAGAAAGTTATATGTATGGTTTCCCTGTTCTACTATACATAACGTTAAAGT ACACCTTCTTTGTTAAAAATGTACTTGCTAAACTTCAGCGTAAATAAAAACATTTTGACTTTG AGCGGACCGACTTACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCC CAACCTGCCATCACGAGATTTCGATTCCACCGCCGC
Restriction Sites	SgfI-RsrII
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_053281.3
Summary	This gene is one of two genes which encode a protein similar to the Drosophila protein dachshund, a transcription factor involved in cell fate determination in the eye, limb and genital disc of the fly. The encoded protein contains two characteristic dachshund domains: an N-terminal domain responsible for DNA binding and a C-terminal domain responsible for protein-protein interactions. This gene is located on the X chromosome and is subject to inactivation by DNA methylation. The encoded protein may be involved in regulation of organogenesis and myogenesis, and may play a role in premature ovarian failure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
Locus ID	117154
MW	19

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