EHHADH (NM_001966) Human 3' UTR Clone

CAT#: SC215685

3' UTR clone of enoyl-Coenzyme A hydratase/3-hydroxyacyl Coenzyme A dehydrogenase (EHHADH) for miRNA target validation



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CNY 5,795.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


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

CNY 1,280.00

Specifications

Product Data
Product Name EHHADH (NM_001966) Human 3' UTR Clone
Vector pMirTarget
Synonyms ECHD; FRTS3; L-PBE; LBFP; LBP; MFE1; PBFE
ACCN NM_001966
Insert Size 1632 bp
Sequence Data
>SC215685 3’UTR clone of NM_001966
The sequence shown below is from the reference sequence of NM_001966. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
TTGGCAGGCTCCCCTAGCAGTAAATTGTGATTCAGTCTTCCAGATTATGCCTCACATGCTAGCATCAGG
TAATGCTGACTGAATTTCAGTGAAATTAAATCAAAAATCCAAAGTAAGATTGTTCTGAAATACAAAGCA
AAATAAATAATCATTAGAATCTTCTGTGTAACGACTCTAATGGTCAAATCTTTAGGAATGTGCTTCCTA
TGCCTCTGAATCTGTCCTTATCAGATAAATTCAATGCATGAACTTGTGTGAATATAATACCATAATAGC
TAATGAAAGAGGCTCAGGCATAAGTTGAGATTCTCAAATGCTTTTATCATTGGATAAATGTGTCATCAA
TTAATAAATGATAAATGCAGCTAAGTCATACATTCATTTTGACTCCTTTCAATGTCACACACATAGTAT
TGATCAGAAATCTTATGAATCATACATACACTCAACAAACATTAAAGTTGTAGGAAAAAGACAGTTGGA
AATTGGTAAGGGAACTGAGTACTTCAAACCAGCACAGGGAACTTAGGTTAGTGTGGCAAGCCTTTCCTC
TTCTGGTCTTTCCTCTTCTGTTTATGGAGAAATAATAGAAAGTAGTAAGTCGTTAACTTAGTGTAAGAA
GGGTCTTAGAGAACATCTAACCTTCTAGGATTTCCCAATTCTGTGATAGAGTAATGACACCAGTTTTCC
TGTCATGACAAGCCTCTGTGATGTTACATATGGAAATGGTTGAATCTTGAAAAATCTAAAATTGTTGCA
AAACATATTTTGTATGATTTTGTTGTAAGAGTTCTTCTCTTTTTACTTTTTGCCTTGTGTAGTTAAAAA
TTAAGGGGCTGGTCAATACAAAAACTTGTACACAAATATTTATAGCAGAATTATTCATAATGGCCAAAA
GCTGAATACAACCCAAATGTCTATGAACTAATGAATAGATAAACCAAATCTGGTATATCCATACAATGG
ACTATATTATTCAGCCATAAAAAGAAATAAAGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCAC
TTTGGGAGGCTGAGGCAGGAGGATTGTTTGAGGCCAGAAATTTGAGACCAGCCTGGGCAACATAGCAAA
ACCCTGTCTCTACAAAAAATACTTTCCGTACATTAGTGGTTGCCTAAGGCTAGAATTGGGGGTGATGAA
TGGGGAGTACAGGATTCATCTAATGGGTACAGGATTTCTTTATGGTTCATGAAAATGGTCTAAACTTAT
TGTGGTAATGGTCACATAACAATATATTAAAAACCATTGAGTTGTATATTTTAAGTGGGTGAATTATAT
GGTATGTGAATTATATCTCAATAAAGTTGTTAGTAAATAAATGGGGCTGAAGATGTTATCCTTCATTGT
GGTGTAAATGAACTTTCACAATATTTTCACCTGTGAACCCAAATAAAATGATTAAAGTTCTGATGGAAA
AATCTTGAATGGAGTATAAGTTTTCCGTTGTTAAAAAGCAAACAAAAAACCAACAAAAAATCCAAGTGT
GCCTTGAATTGTACAGAGCACAATTATTATGTTTGAAATGTGTACTACTTAATTTTATATAATTTGGTT
TGTGAAATTAAAGACATCAATAAAAATGATTCCTGAAAGTAGTAA
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_001966.4
Synonyms ECHD; FRTS3; L-PBE; LBFP; LBP; MFE1; PBFE
Summary The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
Locus ID 1962
MW 63.1
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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