HGF (NM_000601) Human 3' UTR Clone

Specifications

Product Data
Product Name	HGF (NM_000601) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DFNB39; F-TCF; HGFB; HPTA; SF
ACCN	NM_000601
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC206339 3’UTR clone of NM_000601 The sequence shown below is from the reference sequence of NM_000601. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TAAGGTACCACAGTCATAGCTGAAGTAAGTGTGTCTGAAGCACCCACCAATACAACTGTCTTTTACATG AAGATTTCAGAGAATGTGGAATTTAAAATGTCACTTACAACAATCCTAAGACAACTACTGGAGAGTCAT GTTTGTTGAAATTCTCATTAATGTTTATGGGTGTTTTCTGTTGTTTTGTTTGTCAGTGTTATTTTGTCA ATGTTGAAGTGAATTAAGGTACATGCAAGTGTAATAACATATCTCCTGAAGATACTTGAATGGATTAAA AAAACACACAGGTATATTTGCTGGATGATAAAGATTTCATGGGAAAAAAAATCAATTAATCTGTCTAAG CTGCTTTCTGATGTTGGTTTCTTAATAATGAGTAAACCACAAATTAAATGTTATTTTAACCTCACCAAA ACAATTTATACCTTGTGTCCCTAAATTGTAGCCC 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_000601.6
Synonyms	DFNB39; F-TCF; HGFB; HPTA; SF
Summary	This gene encodes a protein that binds to the hepatocyte growth factor receptor to regulate cell growth, cell motility and morphogenesis in numerous cell and tissue types. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate alpha and beta chains, which form the mature heterodimer. This protein is secreted by mesenchymal cells and acts as a multi-functional cytokine on cells of mainly epithelial origin. This protein also plays a role in angiogenesis, tumorogenesis, and tissue regeneration. Although the encoded protein is a member of the peptidase S1 family of serine proteases, it lacks peptidase activity. Mutations in this gene are associated with nonsyndromic hearing loss. [provided by RefSeq, Nov 2015]
Locus ID	3082
MW	17.2

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