HFE (NM_139009) Human 3' UTR Clone

Specifications

Product Data
Product Name	HFE (NM_139009) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	HFE1; HH; HLA-H; MVCD7; TFQTL2
ACCN	NM_139009
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC211814 3’UTR clone of NM_139009 The sequence shown below is from the reference sequence of NM_139009. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGGCACTACGTCTTAGCTGAACGTGAGTGACACGCAGCCTGCAGACTCACTGTGGGAAGGAGACAAAAC TAGAGACTCAAAGAGGGAGTGCATTTATGAGCTCTTCATGTTTCAGGAGAGAGTTGAACCTAAACATAG AAATTGCCTGACGAACTCCTTGATTTTAGCCTTCTCTGTTCATTTCCTCAAAAAGATTTCCCCATTTAG GTTTCTGAGTTCCTGCATGCCGGTGATCCCTAGCTGTGACCTCTCCCCTGGAACTGTCTCTCATGAACC TCAAGCTGCATCTAGAGGCTTCCTTCATTTCCTCCGTCACCTCAGAGACATACACCTATGTCATTTCAT TTCCTATTTTTGGAAGAGGACTCCTTAAATTTGGGGGACTTACATGATTCATTTTAACATCTGAGAAAA GCTTTGAACCCTGGGACGTGGCTAGTCATAACCTTACCAGATTTTTACACATGTATCTATGCATTTTCT GGACCCGTTCAACTTTTCCTTTGAATCCTCTCTCTGTGTTACCCAGTAACTCATCTGTCACCAAGCCTT GGGGATTCTTCCATCTGATTGTGATGTGAGTTGCACAGCTATGAAGGCTGTACACTGCACGAATGGAAG AGGCACCTGTCCCAGAAAAAGCATCATGGCTATCTGTGGGTAGTATGATGGGTGTTTTTAGCAGGTAGG AGGCAAATATCTTGAAAGGGGTTGTGAAGAGGTGTTTTTTCTAATTGGCATGAAGGTGTCATACAGATT TGCAAAGTTTAATGGTGCCTTCATTTGGGATGCTACTCTAGTATTCCAGACCTGAAGAATCACAATAAT TTTCTACCTGGTCTCTCCTTGTTCTGATAATGAAAATTATGATAAGGATGATAAAAGCACTTACTTCGT GTCCGACTCTTCTGAGCACCTACTTACATGCATTACTGCATGCACTTCTTACAATAATTCTATGAGATA GGTACTATTATCCCCATTTCTTTTTTAAATGAAGAAAGTGAAGTAGGCCGGGCACGGTGGCTCACGCCT GTAATCCCAGCACTTTGGGAGGCCAAAGCGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCT AACATGGTGAAACCCCATCTCTAATAAAAATACAAAAAATTAGCTGGGCGTGGTGGCAGACGCCTGTAG TCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATGGCATGAACCCAGGAGGCAGAGCTTGCAGTGAGCCG AGTTTGCGCCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCCATCTCAAAAAAATAAAAATAAAAA TAAAAAAATGAAAAAAAAAAGAAAGTGAAGTATAGAGTATCTCATAGTTTGTCAGTGATAGAAACAGGT TTCAAACTCAGTCAATCTGACCGTTTGATACATCTCAGACACCACTACATTCAGTAGTTTAGATGCCTA GAATAAATAGAGAAGGAAGGAGATGGCTCTTCTCTTGTCTCATTGTGTTTCTTCTGAGTGAGCTTGAAT CACATGAAGGGGAACAGCAGAAAACAACCAACTGATCCTCAGCTGTCATGTTTCCTTTAAAAGTCCCTG AAGGAAGGTCCTGGAATGTGACTCCCTTGCTCCTCTGTTGCTCTCTTTGGCATTCATTTCTTTGGACCC TACGCAAGGACTGTAATTGGTGGGGACAGCTAGTGGCCCTGCTGGGCTTCACACACGGTGTCCTCCCTA GGCCAGTGCCTCTGGAGTCAGAACTCTGGTGGTATTTCCCTCAATGAAGTGGAGTAAGCTCTCTCATTT TGAGATGGTATAATGGAAGCCACCAAGTGGCTTAGAGGATGCCCAGGTCCTTCCATGGAGCCACTGGGG TTCCGGTGCACATTAAAAAAAAAATCTAACCAGGACATTCAGGAATTGCTAGATTCTGGGAAATCAGTT CACCATGTTCAAAAGAGTCTTTTTTTTTTTTTTGAGACTCTATTGCCCAGGCTGGAGTGCAATGGCAT 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_139009.3
Synonyms	HFE1; HH; HLA-H; MVCD7; TFQTL2
Summary	The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]
Locus ID	3077
MW	75.5

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