NDUFS8 antibody (AA 35-210)

Catalog No. ABIN6144496

The Rabbit Polyclonal anti-NDUFS8 antibody (ABIN6144496) specifically detects NDUFS8 in WB, IHC and IF. The antibody is reactive with Human samples.

Quick Overview for NDUFS8 antibody (AA 35-210) (ABIN6144496)

Target: NDUFS8 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 8, 23kDa (NADH-Coenzyme Q Reductase) (NDUFS8))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NDUFS8 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-NDUFS8 Antibody

Binding Specificity: AA 35-210

Sequence: TYKYVNMQDP EMDMKSVTDR AARTLLWTEL FRGLGMTLSY LFREPATINY PFEKGPLSPR FRGEHALRRY PSGEERCIAC KLCEAICPAQ AITIEAEPRA DGSRRTTRYD IDMTKCIYCG FCQEACPVDA IVEGPNFEFS TETHEELLYN KEKLLNNGDK WEAEIAANIQ ADYLYR

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 35-210 of human NDUFS8 (NP_002487.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IHC,1:50 - 1:100,IF,1:50 - 1:100

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

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 NDUFS8

Target: NDUFS8 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 8, 23kDa (NADH-Coenzyme Q Reductase) (NDUFS8))

Alternative Name: NDUFS8

Background: This gene encodes a subunit of mitochondrial NADH:ubiquinone oxidoreductase, or Complex I, a multimeric enzyme of the respiratory chain responsible for NADH oxidation, ubiquinone reduction, and the ejection of protons from mitochondria. The encoded protein is involved in the binding of two of the six to eight iron-sulfur clusters of Complex I and, as such, is required in the electron transfer process. Mutations in this gene have been associated with Leigh syndrome.,NDUFS8,CI-23k,CI23KD,TYKY,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFS8

Molecular Weight: 23 kDa

Gene ID: 4728

UniProt: O00217