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NDUFAF2 antibody (AA 1-169)
NDUFAF2
Reactivity: Human
WB, IF
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-NDUFAF2 Antibody
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Target
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NDUFAF2
(NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))
Binding Specificity
All epitopes for NDUFAF2 antibodies
AA 1-169
Reactivity
All reactivities for NDUFAF2 antibodies
Human
Host
All hosts for NDUFAF2 antibodies
Rabbit
Clonality
All clonalities for NDUFAF2 antibodies
Polyclonal
Conjugate
All conjugates for NDUFAF2 antibodies
This NDUFAF2 antibody is un-conjugated
Application
All applications for NDUFAF2 antibodies
Western Blotting (WB), Immunofluorescence (IF)
Purpose
NDUFAF2 Rabbit pAb
Sequence
MGWSQDLFRA LWRSLSREVK EHVGTDQFGN KYYYIPQYKN WRGQTIREKR IVEAANKKEV DYEAGDIPTE WEAWIRRTRK TPPTMEEILK NEKHREEIKI KSQDFYEKEK LLSKETSEEL LPPPVQTQIK GHASAPYFGK EEPSVAPSST GKTFQPGSWM PRDGKSHNQ
Cross-Reactivity
Human, Mouse, Rat
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-169 of human NDUFAF2 (NP_777549.1).
Isotype
IgG
Top Product
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Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000,IF,1:50 - 1:200
Restrictions
For Research Use only
Handling
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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.
Target Details for NDUFAF2
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Target
NDUFAF2
(NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))
Alternative Name
NDUFAF2 (NDUFAF2 Products )
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.,NDUFAF2,B17.2L,MMTN,NDUFA12L,mimitin,Cancer,Tumor biomarkers,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,NDUFAF2
Molecular Weight
19kDa
Gene ID
91942
UniProt
Q8N183
Pathways
SARS-CoV-2 Protein Interactome
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