NDUFS7 Rabbit pAb - A24466

NDUFS7 Rabbit pAb

Sizes: 20μL, 100μL

Catalogue Numbers: A24466-20, A24466-100

Citations, Manuals and MSDS Available upon request.

Background: This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH) :ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.

Category: Polyclonal Antibodies

Applications: WB, ELISA

Cross-reactivity: Human

Protein Weight: 22kDa/23kDa

Observed Molecular Weight: 20kDa

Immunogen: Synthetic peptide .

Species: human

GeneID: 374291

SWISS: O75251

Alternate Names: NDUFS7; CI-20; CI-20KD; MY017; PSST; NADH:ubiquinone oxidoreductase core subunit S7

Source: Rabbit

Isotype: IgG

Purity: Affinity purification

Storage: Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol, preserved with proclin300 or sodium azide (as specified on the Certificate of Analysis),  pH 7.3.

Recommended Dilutions: WB, 1:1000 - 1:5000 ELISA, Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.

Research Areas: Cancer, Signal Transduction, Endocrine & Metabolism, Mitochondrial metabolism, Mitochondrial markers, Oxidative phosphorylation, Neuroscience, Neurodegenerative Diseases.

NCBI Alias: NDUFS7

Research Use Only