GTX46352
COQ2 antibody, Internal
Cannot supply to this region.
- SKU:
- GTX46352
- Additional Names:
- coenzyme Q2, polyprenyltransferase , CL640 , COQ10D1 , MSA1 , PHB:PPT
- Application:
- WB
- Concentration:
- 0.5-1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 2% Sucrose, 0.09% Sodium azide.
- Immunogen:
- A synthetic peptide corresponding to an Internal region of Human COQ2
- Synonyms:
- 4-HB polyprenyltransferase;4-hydroxybenzoate decaprenyltransferase;4-hydroxybenzoate polyprenyltransferase, mitochondrial;CL640;coenzyme Q2 4-hydroxybenzoate polyprenyltransferase;coenzyme Q2 homolog, prenyltransferase;COQ10D1;MSA1;para-hydroxybenzoate-polyprenyltransferase, mitochondrial;PHB:polyprenyltransferase;PHB:PPT
- Extra Details:
- 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]
- Shipping Conditions:
- Blue Ice