SDHA antibody

Catalog No. ABIN7260583

Product Details anti-SDHA Antibody

Target: SDHA (Succinate Dehydrogenase Complex, Subunit A, Flavoprotein (Fp) (SDHA))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SDHA antibody is un-conjugated

Application: Immunohistochemistry (IHC), Immunofluorescence (IF)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human SDHA (NP_004159.2).

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:200 IF 1:10-1:100

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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 SDHA

Target: SDHA (Succinate Dehydrogenase Complex, Subunit A, Flavoprotein (Fp) (SDHA))

Alternative Name: SDHA (SDHA Products)

Synonyms: CG17246 antibody, Dmel\\CG17246 antibody, Scs-fp antibody, Sdh antibody, Sdha antibody, scs-fp antibody, sdh antibody, CMD1GG antibody, FP antibody, PGL5 antibody, SDH1 antibody, SDH2 antibody, SDHF antibody, 1500032O14Rik antibody, 2310034D06Rik antibody, 4921513A11 antibody, C81073 antibody, im:7141001 antibody, zgc:56051 antibody, Fp antibody, sdha-b antibody, Succinate dehydrogenase, subunit A (flavoprotein) antibody, succinate dehydrogenase complex flavoprotein subunit A antibody, succinate dehydrogenase complex, subunit A, flavoprotein (Fp) antibody, succinate dehydrogenase complex subunit A, flavoprotein (Fp) S homeolog antibody, SdhA antibody, SDHA antibody, Sdha antibody, sdha antibody, sdha.S antibody

Background: This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Gene ID: 6389

UniProt: P31040