anti-Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) Antibodies

COQ2 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. Additionally we are shipping COQ2 Kits (7) and COQ2 Proteins (4) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
COQ2 27235 Q96H96
COQ2 498332 Q499N4
COQ2 71883  
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Top anti-COQ2 Antibodies at antibodies-online.com

Showing 6 out of 7 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Delivery Price Details
Dog Rabbit Un-conjugated WB WB Suggested Anti-COQ2 Antibody Titration:  0.2-1 ug/ml  ELISA Titer:  1:12500  Positive Control:  DU145 cell lysate COQ2 is supported by BioGPS gene expression data to be expressed in DU145 Host:  Rabbit  Target Name:  COQ2  Sample Tissue:  Human MCF7  Antibody Dilution:  1.0ug/ml 100 μL 2 to 3 Days
$319.00
Details
Human Rabbit Un-conjugated WB 100 μL 11 to 14 Days
$581.17
Details
Human Mouse Un-conjugated ELISA, WB Western Blot detection against Immunogen (31.13 KDa) . 100 μg 11 to 12 Days
$440.00
Details
Human Mouse Un-conjugated ELISA, WB   100 μg 11 to 14 Days
$837.83
Details
Human Rabbit Un-conjugated WB COQ2 antibody used at 1 ug/ml to detect target protein. 50 μg 9 to 11 Days
$449.29
Details
Caenorhabditis elegans Chicken Un-conjugated WB   100 μg 6 to 8 Days
$646.71
Details

Top referenced anti-COQ2 Antibodies

  1. Dog (Canine) Polyclonal COQ2 Primary Antibody for WB - ABIN2782857 : Diomedi-Camassei, Di Giandomenico, Santorelli, Caridi, Piemonte, Montini, Ghiggeri, Murer, Barisoni, Pastore, Muda, Valente, Bertini, Emma: COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement. in Journal of the American Society of Nephrology : JASN 2007 (PubMed)
    Show all 2 Pubmed References

More Antibodies against COQ2 Interaction Partners

Fruit Fly (Drosophila melanogaster) Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) interaction partners

  1. flies defective in CoQ biosynthetic gene coq2 were more susceptible to bacterial and fungal infections, while were more resistant to viruses

  2. sbo is an essential gene for Drosophila development, mutation of which leads to an extension of lifespan most likely by altering endogenous CoQ biosynthesis.

Human Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) interaction partners

  1. Results suggest that COQ2 is not a genetic risk factor for multiple system atrophy in Italian population.

  2. CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 homozygous variant p.Gly390Ala was identified by Next Generation Sequencing in two cousins.

  3. Recessive causative mutations in COQ2 are very rare in Italian multiple system atrophy patients.

  4. We defined the structure of COQ2 with relevant implications for mutation screening in patients and demonstrated that, contrary to other COQ gene defects such as ADCK3, there is a correlation between COQ2 genotype and patient's phenotype.

  5. Findings provide evidence that the previously reported association of COQ2 V393A polymorphism with increased risk of multiple system atrophy in Japanese also applies to Han Chinese, as well as more broadly to other East Asian populations

  6. The V393A variant in the COQ2 gene increases risk of PD.

  7. Results indicated that COQ2 tended to play a population-specific and subtype-depended role in conferring susceptibility to multiple system atrophy

  8. This case-control study shows no evidence for an association between ALS and the V393A variant of COQ2 in Han Chinese.

  9. This study demonstrated that COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese.

  10. Multiple system atrophy due to recessive COQ2 mutations (including exon dosage) was not observed in our study

  11. The recessive COQ2 mutations recently were nominated to be the genetic cause in a subset of familial and sporadic MSA cases.

  12. A novel homozygous mutation in COQ2 (c.905C>T,p.Ala302Val) found in dizygotic twins is linked to fatal infantile multisystem disease.

  13. Functionally impaired variants of COQ2 were associated with an increased risk of multiple-system atrophy in multiplex families and patients with sporadic disease.

  14. [review] Primary CoQ10 deficiency is due to defects in CoQ10 biosynthesis, while secondary forms are due to other causes.

  15. Treatment with CoQs having shorter isoprenoid chains, especially CoQ2, induced apoptosis in p53-point mutated BALL-1 cells, whereas treatment with longer isoprenoid chains did not.

  16. Substitution of a highly conserved tyrosine to cysteine at amino acid 297 of COQ2 is the first molecular cause of primary CoQ(10) deficiency.

  17. We have found that both 3-[(cholamidopropyl)dimethylammonio]-1-propanesulfonate and sodium cholate, but not sodium deoxycholate, lysophosphatidyl choline, or octylglucoside, significantly stimulate ubiquinone activity over that measured with Triton X-100.

  18. Our results support a requirement for CoQ(10) to control superoxide levels in HL-60 cells.

  19. A deletirious frame shift deletion mutation that causes severe ubiquinone deficiency was identified in COQ2.

  20. Study is the first direct demonstration of the pathogenicity of a COQ2 mutation involved in human disease, and establishes yeast as a useful model to study human CoQ(10) deficiency.

Mouse (Murine) Coenzyme Q2 Homolog, Prenyltransferase (Yeast) (COQ2) interaction partners

  1. Calorie restriction modifies ubiquinone and COQ transcript levels in mouse tissues

COQ2 Antigen Profile

Protein 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.

Gene names and symbols associated with COQ2

  • Coenzyme Q biosynthesis protein 2 (Coq2) antibody
  • coenzyme Q2, polyprenyltransferase (COQ2) antibody
  • coenzyme Q2, polyprenyltransferase (Coq2) antibody
  • coenzyme Q2 4-hydroxybenzoate polyprenyltransferase (coq2) antibody
  • coenzyme Q2 4-hydroxybenzoate polyprenyltransferase (Coq2) antibody
  • 4-hydroxybenzoate polyprenyltransferase, mitochondrial (coq-2) antibody
  • 2310002F18Rik antibody
  • CG9613 antibody
  • CL640 antibody
  • coq2 antibody
  • COQ10D1 antibody
  • Dmel\\CG9613 antibody
  • MSA1 antibody
  • RGD1306722 antibody
  • sbo antibody
  • zgc:162600 antibody

Protein level used designations for COQ2

CG9613-PA , Coq2-PA , coenzyme Q biosynthesis protein 2 , small boy , 4-hydroxybenzoate polyprenyltransferase, mitochondrial , PHB:polyprenyltransferase , coenzyme Q2 homolog, prenyltransferase , para-hydroxybenzoate-polyprenyltransferase, mitochondrial , para-hydroxybenzoate--polyprenyltransferase, mitochondrial

GENE ID SPECIES
40988 Drosophila melanogaster
27235 Homo sapiens
498332 Rattus norvegicus
100037331 Danio rerio
478457 Canis lupus familiaris
71883 Mus musculus
504633 Bos taurus
175969 Caenorhabditis elegans
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