COQ10A Polyclonal antibody

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  WB analysis using 29496-1-AP

  Various lysates were subjected to SDS PAGE followed by western blot with 29496-1-AP (COQ10A antibody) at dilution of 1:20000 incubated at room temperature for 1.5 hours.

COQ10A Polyclonal Antibody for WB, ELISA

Cat No. 29496-1-AP

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, ELISA

Synonyms

Coenzyme Q-binding protein COQ10 homolog A, mitochondrial

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Tested Applications

• Positive WB detected in: mouse heart tissue, mouse skeletal muscle tissue, rat heart tissue, rat skeletal muscle tissue

Recommended dilution

• Western Blot (WB): WB : 1:5000-1:50000

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, Check data in validation data gallery.

Product Information

29496-1-AP targets COQ10A in WB, ELISA applications and shows reactivity with human, mouse, rat samples.

• Tested Reactivity: human, mouse, rat
• Host / Isotype: Rabbit / IgG
• Class: Polyclonal
• Type: Antibody
• Immunogen: COQ10A fusion protein Ag31534
• Full Name: coenzyme Q10 homolog A (S. cerevisiae)
• Calculated Molecular Weight: 28KD
• Observed Molecular Weight: 20 kDa
• GenBank Accession Number: NM_144576
• Gene Symbol: COQ10A
• Gene ID (NCBI): 93058
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Antigen affinity purification
• UNIPROT ID: Q96MF6
• Storage Buffer: PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
• Storage Conditions: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20^oC storage. 20ul sizes contain 0.1% BSA.

Background Information

COQ10A is a human gene that encodes a protein involved in the biosynthesis of coenzyme Q10 (CoQ10), also known as ubiquinone. CoQ10 is a lipid-soluble antioxidant and a critical component of the mitochondrial electron transport chain, where it plays a key role in cellular energy production (ATP synthesis). Mutations or deficiencies in COQ10A have been implicated in primary CoQ10 deficiency syndromes, which can manifest as mitochondrial disorders such as encephalomyopathy, nephropathy, and Leigh syndrome.