Anti-Human/Mouse NDUFA12 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA11361
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human NDUFA12
Specificity
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot Q9UI09
Concentration 0.4 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names 13 kDa differentiation associated protein,13 kDa differentiation-associated protein,2410011G03Rik,AW112974,B17.2,CI-B17.2,CIB17.2,Complex I B17.2,Complex I B17.2 subunit,Complex I-B17.2,DAP13,MGC107642,MGC7999,NADH dehydrogenase (ubiquinone) 1 alpha subcomplex 12,NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12,NADH ubiquinone oxidoreductase subunit B17.2,NADH-ubiquinone oxidoreductase subunit B17.2,NDUAC,NDUFA12,RGD1311462
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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