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
Cited in 1 publication. |
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经常一起买 (2)
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 |
Citations (1)
The use of this cDNA Clones has been cited in the following citations: |
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A Personalized Model of COQ2 Nephropathy Rescued by the Wild-Type COQ2 Allele or Dietary Coenzyme Q10 Supplementation
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Journal of the American Society of Nephrology : JASN
,PubMed ID 28428331
[COQ2]
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