NDUFA2 antibody (AA 1-95)
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- Target See all NDUFA2 Antibodies
- NDUFA2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, 2, 8kDa (NDUFA2))
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Binding Specificity
- AA 1-95
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This NDUFA2 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- Sequence
- MAAAAASRGV GAKLGLREIR IHLCQRSPGS QGVRDFIEKR YVELKKANPD LPILIRECSD VQPKLWARYA FGQETNVPLN NFSADQVTRA LENVL
- Cross-Reactivity
- Human, Mouse, Rat
- Characteristics
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-95 of human NDUFA2 (NP_002479.1).
- Isotype
- IgG
- Top Product
- Discover our top product NDUFA2 Primary Antibody
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- Application Notes
- WB,1:500 - 1:2000,IF,1:50 - 1:200
- Comment
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HIGH QUALITY
- Restrictions
- For Research Use only
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- Format
- Liquid
- 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
- 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. Alternative splicing results in multiple transcript variants.,NDUFA2,B8,CD14,CIB8,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFA2
- Molecular Weight
- 8 kDa/10 kDa
- Gene ID
- 4695
- UniProt
- O43678
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