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NDUFA2 antibody
NDUFA2
Reactivity: Human, Mouse
ELISA, WB, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-NDUFA2 Antibody
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Target
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NDUFA2
(NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 2, 8kDa (NDUFA2))
Reactivity
All reactivities for NDUFA2 antibodies
Human, Mouse
Host
All hosts for NDUFA2 antibodies
Rabbit
Clonality
All clonalities for NDUFA2 antibodies
Polyclonal
Conjugate
All conjugates for NDUFA2 antibodies
This NDUFA2 antibody is un-conjugated
Application
All applications for NDUFA2 antibodies
ELISA, Western Blotting (WB), Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant protein of human NDUFA2
Isotype
IgG
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Discover our top product NDUFA2 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB 1:500-1:2000, IHC 1:25-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.4 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for NDUFA2
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Target
NDUFA2
(NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 2, 8kDa (NDUFA2))
Alternative Name
NDUFA2 (NDUFA2 Products )
Synonyms
NDUFA2 antibody, b8 antibody, cd14 antibody, cib8 antibody, AV000592 antibody, B8 antibody, C1-B8 antibody, CI-B8 antibody, CD14 antibody, CIB8 antibody, NADH:ubiquinone oxidoreductase subunit A2 antibody, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2 antibody, Ndufa2 antibody, NDUFA2 antibody, ndufa2 antibody
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.
Molecular Weight
11 kDa
UniProt
O43678
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