NDUFAF2 antibody
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- Target See all NDUFAF2 Antibodies
- NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This NDUFAF2 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Recombinant fusion protein of human NDUFAF2 (NP_777549.1).
- Isotype
- IgG
- Top Product
- Discover our top product NDUFAF2 Primary Antibody
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- Application Notes
- WB 1:500-1:2000 IF 1:50-1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- 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.
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- Target
- NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))
- Alternative Name
- NDUFAF2 (NDUFAF2 Products)
- Synonyms
- B17.2L antibody, MMTN antibody, NDUFA12L antibody, mimitin antibody, Ndufa12l antibody, RGD1560158 antibody, NDUFAF2 antibody, ndufa12l antibody, zgc:101036 antibody, 1810058I14Rik antibody, C86051 antibody, NADH:ubiquinone oxidoreductase complex assembly factor 2 antibody, NADH:ubiquinone oxidoreductase complex assembly factor 2 L homeolog antibody, NADH dehydrogenase (ubiquinone) complex I, assembly factor 2 antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 2 antibody, NDUFAF2 antibody, Ndufaf2 antibody, ndufaf2.L antibody, ndufaf2 antibody
- 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.
- Molecular Weight
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Observed_MW: 20 kDa
Calculated_MW: 19 kDa
- Gene ID
- 91942
- UniProt
- Q8N183
- Pathways
- SARS-CoV-2 Protein Interactome
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