COQ2 (NM_015697) Human 3' UTR Clone

CAT#: SC205261

3' UTR clone of coenzyme Q2 homolog prenyltransferase (yeast) (COQ2) nuclear gene encoding mitochondrial protein for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Cited in 1 publication.

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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 COQ2 (NM_015697) Human 3' UTR Clone
Vector pMirTarget
Synonyms CL640; COQ10D1; MSA1; PHB:PPT
ACCN NM_015697
Insert Size 405 bp
Sequence Data
>SC205261 3’UTR clone of NM_015697
The sequence shown below is from the reference sequence of NM_015697. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
AAGGGTATAGAGAATAAAATAGAAAATTAATGAATGAAATTTATCTAGGAATTTTTAAAACATTTTTTA
CAAAATATAATTAGATTTGAATACAAAATCTGATACAATATGTTAAAGAATTAAGAACCTGAAGATGAA
GATTTAGAGCATATTTACCTGGATTTTACTTATTTGCTAGCAAAATTCCCCCTTGTCACAGAAACCAGG
GACTCTTCAGGATTTGAGATGGCCTTGAGTATTTTAGTTGATACATTCTTCTGCCCATTATAATTCTCA
CCTGAAGTTATGGGGATTGCACGGGTTTTGGCACTTTAGAAAAAGCCTGATGTGGGTCTTACATAAATG
AATGTCTGTATAAGAAAATGGACTCTTTTTTTTAGGGAAAAATAAAAGCAACTATGGGAA
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_015697.9
Synonyms CL640; COQ10D1; MSA1; PHB:PPT
Summary This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme, which is part of the coenzyme Q10 pathway, catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency, a mitochondrial encephalomyopathy, and also COQ2 nephropathy, an inherited form of mitochondriopathy with primary renal involvement. [provided by RefSeq, Oct 2009]
Locus ID 27235
MW 16.1
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Citations (1)

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