NDUFA12 antibody

Catalog No. ABIN7237961

Product Details anti-NDUFA12 Antibody

Target: NDUFA12 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 12 (NDUFA12))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFA12 antibody is un-conjugated

Application: ELISA, Immunohistochemistry (IHC)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Synthetic peptide of human NDUFA12

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.6 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for NDUFA12

Target: NDUFA12 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 12 (NDUFA12))

Alternative Name: NDUFA12 (NDUFA12 Products)

Synonyms: RGD1311462 antibody, si:dkey-183c16.3 antibody, zgc:112053 antibody, B17.2 antibody, DAP13 antibody, 2410011G03Rik antibody, AW112974 antibody, NADH:ubiquinone oxidoreductase subunit A12 antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12 antibody, Ndufa12 antibody, NDUFA12 antibody, ndufa12 antibody

Background: This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants.

NCBI Accession: NP_061326

UniProt: Q9UI09