HFE (NM_000410) Human 3' UTR Clone

CAT#: SC211816

3' UTR clone of hemochromatosis (HFE) transcript variant 1 for miRNA target validation


Reconstitution Protocol

USD 683.00

4 Weeks*

Size
    • 10 ug

Product Images

Frequently bought together (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

USD 188.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

USD 160.00

Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol HFE
Synonyms HFE1; HH; HLA-H; MVCD7; TFQTL2
ACCN NM_000410
Insert Size 2000 bp
Sequence Data
>SC211816 3’UTR clone of NM_000410
The sequence shown below is from the reference sequence of NM_000410. 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).
Product Components The cDNA clone is shipped in a 2-D bar-coded Matrix tube as 10 ug dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials.
Reference Data
RefSeq NM_000410.4
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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