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Rabbit
Anti-COQ2/Gold
Cat. Number:
bs-13984R-Gold
Quantity size:
100ul
35nm
Concentration:
0.4mg/ml Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Background:
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]
Also known as:
2310002F18Rik;
4-hydroxybenzoate polyprenyltransferase;
CL640;
Coenzyme Q2 homolog, prenyltransferase (yeast);
COQ2;
COQ2 homolog;
COQ2_HUMAN;
FLJ13014;
FLJ26072;
hCOQ2;
MGC124824;
MGC91278;
mitochondrial;
OTTMUSP00000032111;
Para-hydroxybenzoate--polyprenyltransferase;
Para-hydroxybenzoate--polyprenyltransferase, mitochondrial;
PHB:polyprenyltransferase;
RGD1306722.
Specificity:
●
Rabbit Polyclonal IgG, affinity purified by Protein A.
●
Reacts with:
(predicted: )
●
Immunogen: KLH conjugated synthetic peptide derived from human COQ2.
●
Predicted Molecular Weight: 37kDa.
Storage:
0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300. Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
Application:
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.