ARG56396

anti-NDUFA2 antibody

anti-NDUFA2 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes NDUFA2
Tested Reactivity Hu, Ms
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name NDUFA2
Antigen Species Human
Immunogen Recombinant protein of Human NDUFA2
Conjugation Un-conjugated
Alternate Names CI-B8; Complex I-B8; CD14; NADH-ubiquinone oxidoreductase B8 subunit; CIB8; B8; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:50 - 1:100
WB1:500 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Mouse kidney

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% sodium azide
Stabilizer 50% Glycerol
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: 17991 Mouse NDUFA2

GeneID: 4695 Human NDUFA2

Swiss-port # O43678 Human NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2

Swiss-port # Q9CQ75 Mouse NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2

Gene Symbol NDUFA2
Gene Full Name NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa
Background The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
Function Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. [UniProt]
Calculated MW 11 kDa