ARG65571

anti-NDUFAF2 antibody

anti-NDUFAF2 antibody for Western blot and Human

Cancer antibody; Controls and Markers antibody; Metabolism antibody; Signaling Transduction antibody

Overview

Product Description Rabbit Polyclonal antibody recognizes NDUFAF2
Tested Reactivity Hu
Tested Application WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name NDUFAF2
Antigen Species Human
Immunogen Fusion protein of human NDUFAF2
Conjugation Un-conjugated
Alternate Names B17.2L; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2; mimitin; Myc-induced mitochondrial protein; MMTN; NDUFA12-like protein; NDUFA12L; Mimitin, mitochondrial; B17.2-like

Application Instructions

Application Suggestion
Tested Application Dilution
WB500-2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Raji cell and human liver cancer tissue, HeLa cell

Properties

Form Liquid
Purification Purified by antigen-affinity chromatography.
Buffer 1XPBS (pH 7.4), 0.05% Sodium azide and 40% Glycerol
Preservative 0.05% Sodium azide
Stabilizer 40% Glycerol
Concentration 2.6 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 91942 Human NDUFAF2

Swiss-port # Q8N183 Human Mimitin, mitochondrial

Gene Symbol NDUFAF2
Gene Full Name NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
Background 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.
Function Acts as a molecular chaperone for mitochondrial complex I assembly. [UniProt]
Highlight Related products:
Anti-Rabbit IgG secondary antibodies;
Related poster download:
The Structure & Functions of Mitochondria.pdf
Research Area Cancer antibody; Controls and Markers antibody; Metabolism antibody; Signaling Transduction antibody
Calculated MW 20 kDa