Product Name
4-hydroxybenzoate polyprenyltransferase, mitochondrial (COQ2), ELISA Kit
Full Product Name
Porcine 4-hydroxybenzoate polyprenyltransferase, mitochondrial (COQ2) ELISA Kit
Product Gene Name
COQ2 elisa kit
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Request Current Manual
Species Reactivity
Porcine
Samples
Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate
Preparation and Storage
Store all reagents at 2-8 degree C.
Sample Preparation
We suggest pre-experimenting with neat (undiluted) samples, 1:2 or 1:4 dilutions. Please avoid diluting your samples more than 1:10 as it would exceed the dilution limit set for this kit. If the expected concentration of the target is beyond the detection range of the kit, please contact our technical support team
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of COQ2 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Searchable Terms for COQ2 purchase
MBS7237910 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the 4-hydroxybenzoate polyprenyltransferase, mitochondrial (COQ2) ELISA Kit target analytes in
biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing COQ2. The ELISA analytical biochemical technique of the MBS7237910 kit is based on COQ2 antibody-COQ2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect COQ2 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, COQ2. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
NCBI/Uniprot data below describe general gene information for COQ2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_056512.5
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NCBI GenBank Nucleotide #
NM_015697.7
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UniProt Secondary Accession #
O95331; Q1JQ78; Q684R2[Other Products]
UniProt Related Accession #
Q96H96[Other Products]
Molecular Weight
35,468 Da
NCBI Official Full Name
4-hydroxybenzoate polyprenyltransferase, mitochondrial
NCBI Official Synonym Full Names
coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
NCBI Official Symbol
COQ2??[Similar Products]
NCBI Official Synonym Symbols
MSA1; CL640; COQ10D1
??[Similar Products]
NCBI Protein Information
4-hydroxybenzoate polyprenyltransferase, mitochondrial; PHB:polyprenyltransferase; coenzyme Q2 homolog, prenyltransferase; para-hydroxybenzoate-polyprenyltransferase, mitochondrial
UniProt Protein Name
4-hydroxybenzoate polyprenyltransferase, mitochondrial
UniProt Synonym Protein Names
COQ2 homolog; hCOQ2; Para-hydroxybenzoate--polyprenyltransferase; PHB:polyprenyltransferase
UniProt Gene Name
COQ2??[Similar Products]
UniProt Synonym Gene Names
CL640; hCOQ2; PHB:polyprenyltransferase??[Similar Products]
UniProt Entry Name
COQ2_HUMAN
NCBI Summary for COQ2
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]
UniProt Comments for COQ2
COQ2: Catalyzes the prenylation of para-hydroxybenzoate (PHB) with an all-trans polyprenyl group. Mediates the second step in the final reaction sequence of coenzyme Q (CoQ) biosynthesis, which is the condensation of the polyisoprenoid side chain with PHB. Defects in COQ2 are the cause of coenzyme Q10 deficiency, primary, type 1 (COQ10D1). An autosomal recessive disorder with variable manifestations consistent with 5 major phenotypes. The phenotypes include an encephalomyopathic form with seizures and ataxia; a multisystem infantile form with encephalopathy, cardiomyopathy and renal failure; a predominantly cerebellar form with ataxia and cerebellar atrophy; Leigh syndrome with growth retardation; and an isolated myopathic form. Belongs to the UbiA prenyltransferase family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Mitochondrial; Transferase; EC 2.5.1.39; Membrane protein, integral; Membrane protein, multi-pass; Cofactor and Vitamin Metabolism - ubiquinone and other terpenoid-quinone biosynthesis
Chromosomal Location of Human Ortholog: 4q21.23
Cellular Component: mitochondrial inner membrane; integral to membrane
Molecular Function: 4-hydroxybenzoate decaprenyltransferase activity; 4-hydroxybenzoate nonaprenyltransferase activity
Biological Process: ubiquinone biosynthetic process; isoprenoid biosynthetic process; glycerol metabolic process
Disease: Multiple System Atrophy 1, Susceptibility To; Coenzyme Q10 Deficiency, Primary, 1
Research Articles on COQ2
1. The recessive COQ2 mutations recently were nominated to be the genetic cause in a subset of familial and sporadic MSA cases.
Precautions
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