NDUFS6 Antibody - Cat. #: CSB-PA089578

SKU: CSB-PA089578

Size :50ul

Clone Number:

Aliases:BC059730 antibody; CI 13kA antibody; CI 13kD A antibody; CI-13kD-A antibody; CI13KDA antibody; Complex I 13kD A antibody; Complex I 13kDa subunit A antibody; Complex I mitochondrial respiratory chain 13 kD subunit antibody; Complex I-13kD-A antibody; IP13 antibody; MGC107676 antibody; NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH coenzyme Q reductase) antibody; NADH dehydrogenase [ubiquinone] iron sulfur protein 6, mitochondrial antibody; NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial antibody; NADH ubiquinone oxidoreductase 13 kDa A subunit antibody; NADH-ubiquinone oxidoreductase 13 kDa-A subunit antibody; NADH:ubiquinone oxidoreductase NDUFS6 subunit antibody; NADH:ubiquinone oxidoreductase subunit S6 antibody; Ndufs6 antibody; NDUS6_HUMAN antibody

Product Type:Polyclonal Antibody

Immunogen Species:Homo sapiens (Human)

UniProt ID:O75380

Immunogen:Fusion protein of Human NDUFS6

Raised in:Rabbit

Species Reactivity:Human, Mouse, Rat

Tested Applications:ELISA, IHC; ELISA:1:2000-1:5000, IHC:1:50-1:200

Background:This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.

Clonality:Polyclonal

Isotype:IgG

Purification Method:Antigen affinity purification

Conjugate:Non-conjugated

Buffer:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol

Form:Liquid

Stroage:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Target Names:NDUFS6

Research Areas:Cancer;Tags & Cell Markers;Metabolism;Signal transduction