USF1 (NM_007122) Human 3' UTR Clone

Specifications

Product Data
Product Name	USF1 (NM_007122) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	bHLHb11; FCHL; FCHL1; HYPLIP1; MLTF; MLTFI; UEF
ACCN	NM_007122
Insert Size	699 bp
Sequence Data	Insert Sequence (showhide) >SC209086 3’UTR clone of NM_007122 The sequence shown below is from the reference sequence of NM_007122. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGGTCGTCATCAAGAATGACAGCAACTAACTATGGGGATTCAGGGGCTTTGGGCCCAAGAACTGCAGA TAGCCCAGGAGCAACAGCCTAATCCCGTGCCCCTTTCCTTCACTGCCCCACTTCTGGCATGGGACAGGG GGAAGTTCAGAAGGTGTGTCCTTGAACTGAGGCCCTGTGATATGGCGGCCTGCAGTGGTGTGAAACACA CAATGTGGACGTGCACTGACAGCCTTGCCCACCCCCACCATGCAGCCCCTGGGCCCTTGTGCTCCTCTC GCACAATGCATGTGCTGTCTCCATGCTGGATACTGGACACACTAAACTCTGGGGCTTGTCCTGTGCTTG CTTAGAGTGCCCAGCAGAGGTTTGCTGACAGGTGATGCTCTGGCTTGCCCCAGGACTCTGGCACTTCCA TTGGTTCTTCCTTTCCCTGGAGCTGAGGTTTAGATGTGCAACCTGTGGCTCAGGGGAGCAAGCTTACAC AAGAAGTGAGGGAAGGATGTTTAGCAGTGGCTGGTGCCCATGAAGAGGAGATTGGCCAGTGAGAAGCTG AGGCCTATGCAGACATCTCTGGAGCCAGAGAGAACAACAGGCAGGGGCCCACTTGGGGCCTTCCCCCTT GTGGGGGTCGTTTTTTTTTTTTCTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTAAGATAAAATTGT TCAAAGCCA 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_007122.5
Synonyms	bHLHb11; FCHL; FCHL1; HYPLIP1; MLTF; MLTFI; UEF
Summary	This gene encodes a member of the basic helix-loop-helix leucine zipper family, and can function as a cellular transcription factor. The encoded protein can activate transcription through pyrimidine-rich initiator (Inr) elements and E-box motifs. This gene has been linked to familial combined hyperlipidemia (FCHL). Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been defined on chromosome 21. [provided by RefSeq, Feb 2013]
Locus ID	7391
MW	25.8

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