SIX5 (NM_175875) Human 3' UTR Clone

Specifications

Product Data
Product Name	SIX5 (NM_175875) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BOR2; DMAHP
ACCN	NM_175875
Insert Size	746 bp
Sequence Data	Insert Sequence (showhide) >SC209397 3’UTR clone of NM_175875 The sequence shown below is from the reference sequence of NM_175875. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTGCCTGTGGAGGAGCCCTTGGAACTGTGACCCAGTGTGGCCCCGTGGCCTCTCCCGACATTGGTGCTG AAGACGCAGGGACAGGAATGGGAGGGGGGAGCCCCAGAAATGCGGTTGCTGAAGACCCCAGTCACCACA TCCTTCTGCCTGGGTGGCCTCTCCAAGCCCTGGTGGTGCTGGGGGTTGTATCCCCGGCCACCTCCTGTC CAGGTCTCCATCCCCCTTTGGATGGGAGGCCTCTCTGTTACAGCCCTCCCCATGCTGTGCCCTGCCATA TACGTGGGGGACTCAGGGTCCTGACTCAGGGGCCCTGCCCCCTCCACTTGGTACTAGCTGTAAGCGGAA CACCCTGCCCCAGGGCCGGACTTCCAGCCCCCAGAGCCCTCTCCCTGTCACTCCCTGAAACACTATTAA TAGCTCTGCCGATAGCTGGTGTTGTCACAACTGCCTGGAATCCGAAGGTGGAGGACAGGCAGCCCCGCG CCCCTGAGACTGGAGACCCTCCCCAGTGTGGCATTTCCTGCCAGGGGCGGGGGGTGGGGCAGCTGTGGG GAGACGGGGGTCTTCCTTCACCAGCTCCCCTCGACTCAAGCCCTTGTCCTCATTATCCGGCCCAGACCA AAGATTCCCTCATCCCTGGGGGCAGCCCTGCCGCTGTGTCTCCTTTGTATCCTAAATCTTTATTTTTCT AGGACATGTTATGCCTCCATTTTCAATTAAAATAAAGTTATCGGATTACACCACCA 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_175875.5
Synonyms	BOR2; DMAHP
Summary	The protein encoded by this gene is a homeodomain-containing transcription factor that appears to function in the regulation of organogenesis. This gene is located downstream of the dystrophia myotonica-protein kinase gene. Mutations in this gene are a cause of branchiootorenal syndrome type 2. [provided by RefSeq, Jul 2009]
Locus ID	147912
MW	27.1

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