COUP TF1 (NR2F1) (NM_005654) Human 3' UTR Clone

Specifications

Product Data
Product Name	COUP TF1 (NR2F1) (NM_005654) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BBOAS; BBSOAS; COUP-TFI; COUPTF1; EAR-3; EAR3; ERBAL3; SVP44; TCFCOUP1; TFCOUP1
ACCN	NM_005654
Insert Size	799 bp
Sequence Data	Insert Sequence (showhide) >SC203099 3’UTR clone of NM_005654 The sequence shown below is from the reference sequence of NM_005654. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGGCCTTACATGTCCATCCAGTGCTCCTAGACCTTGGGCGCTTCCCACCTGCCCCGTCCCCCTAGAGAC TCAGAGGACCCACCTGGGCCAAGGACTCCAAAGCCGCGGGGACACCGGGAAGTGCAGCGGGCCAGGCAG GCTGGGTGGGAGGGAGGAGGGCCGAGACAGGAGCAGCCCACCCAGCAGAAATACAATCCGAGCTACAAA GCATGGGAAAAAGAGACTCTTTTAGGATCAGATCTGTGAGCACGTTGGCGAGGAAAAACAAAACAAACA AAAAAAAGAACCTTGTGTCTGTCTGGTGAAAAAAAGAAAAACAAATTGGAAGAGAGGACCATGAGAATT TTAATAAAACAGAAGGAAACTAATGGACCTTCCAGGATTTATTGTGGACGGATGTGGATATATTCTGTA CAGGAACAACACATATGGAAGTGGACTGAAGCCTATGTAGAAACACACACACACTGAACATTGTTATTC ATTTTGTAAAATACTAGTCTTTATTTTCATTTTTTGTAAAATTTAAACATCGTATGCGCATAAAGAAAA AGGAAACAAGAATTAGGGGAAAATAACATTTTCCAAATAATTATAAAAAATTGTCCTGTGTCTATGTAT CTATATCTGTTTTGTATTTTTTTCTGGTTCCAAACCAGATTTCCTGTGATTCTATACTAATAATTTTTG ATATAACCCTTTGCTTCTTATAATGAGTGCGATATATGTTGTCGAGGCTGTTCTTCAAGAATTAAAATT GAAGTGAAAATTTAAACAAAAATAAAAGAATTTAGCAAAA 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_005654.6
Synonyms	BBOAS; BBSOAS; COUP-TFI; COUPTF1; EAR-3; EAR3; ERBAL3; SVP44; TCFCOUP1; TFCOUP1
Summary	The protein encoded by this gene is a nuclear hormone receptor and transcriptional regulator. The encoded protein acts as a homodimer and binds to 5'-AGGTCA-3' repeats. Defects in this gene are a cause of Bosch-Boonstra optic atrophy syndrome (BBOAS). [provided by RefSeq, Apr 2014]
Locus ID	7025
MW	31.5

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