Anti-Human/Mouse NDUFAF2 Polyclonal Antibody

NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA09995
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human NDUFAF2
Specificity Highly expressed in ESCC cells. Also expressed in heart, skeletal muscle, liver, and in fibroblasts.
Isotype IgG
Reacitivity Human,Mouse
Clone
Uniprot Q8N183
Concentration 0.6 mg/mL
Dilution WB 1:500-1:2000
Formulation
Application WB,ELISA
Other Names B17.2 like,B17.2-like,B17.2L,FLJ22398,MIMIT,Mimitin,Mimitin mitochondrial,mitochondrial,MMTN,Myc induced mitochondrial protein,Myc-induced mitochondrial protein,NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 2,NADH dehydrogenase (ubiquinone) complex I,assembly factor 2,NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2,NDUFA12 like,NDUFA12 like protein,NDUFA12-like protein,NDUFA12L,NDUFAF2,OTTHUMP00000161882,OTTHUMP00000221703
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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