×
For best experience we recommend to activate Javascript in your browser.
NDUFB3 antibody
NDUFB3
Reactivity: Human, Mouse
IF
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-NDUFB3 Antibody
(hide)
Target
See all NDUFB3 Antibodies
NDUFB3
(NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 3, 12kDa (NDUFB3))
Reactivity
All reactivities for NDUFB3 antibodies
Human, Mouse
Host
All hosts for NDUFB3 antibodies
Rabbit
Clonality
All clonalities for NDUFB3 antibodies
Polyclonal
Conjugate
All conjugates for NDUFB3 antibodies
This NDUFB3 antibody is un-conjugated
Application
All applications for NDUFB3 antibodies
Immunofluorescence (IF)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human NDUFB3 (NP_002482.1).
Isotype
IgG
Top Product
Discover our top product NDUFB3 Primary Antibody
Alternatives
(show)
Application Details
(hide)
Application Notes
IF 1:50-1:100
Restrictions
For Research Use only
Handling
(hide)
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.
Target Details for NDUFB3
(hide)
Target
NDUFB3
(NADH Dehydrogenase (Ubiquinone) 1 beta Subcomplex, 3, 12kDa (NDUFB3))
Alternative Name
NDUFB3 (NDUFB3 Products )
Synonyms
NDUFB3 antibody, 2700033I16Rik antibody, AI415450 antibody, B12 antibody, CI-B12 antibody, NADH:ubiquinone oxidoreductase subunit B3 antibody, NADH:ubiquinone oxidoreductase subunit B3 S homeolog antibody, NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa antibody, NADH dehydrogenase (ubiquinone) 1 beta subcomplex 3 antibody, Ndufb3 antibody, NDUFB3 antibody, ndufb3.S antibody, ndufb3 antibody
Background
This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. This protein localizes to the inner membrane of the mitochondrion as a single-pass membrane protein. Mutations in this gene contribute to mitochondrial complex 1 deficiency. Alternative splicing results in multiple transcript variants encoding the same protein. Humans have multiple pseudogenes of this gene.
Gene ID
4709
UniProt
O43676
Recently viewed
(hide)