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NDUFA12 Antibody

CAT: 0223-23-473Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0223-23-473Size:100 µL
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Background
This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants.
NCBI Gene ID
55967
Swiss Prot
Q9UI09
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-145 of human NDUFA12 (NP_061326.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Neuroscience, Signal Transduction
Purification
Affinity purification
Positive Control
293T
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 17kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:2000
Symbol
NDUFA12
Positive Control 2
PC-12
Positive Control 3
HepG2
Positive Control 4
Mouse kidney
Positive Control 5
Mouse heart
Positive Control 6
Mouse testis
NCBI Official Name
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12
NCBI Organism
Homo sapiens
Other Product Names
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12, 13 kDa differentiation-associated protein, Complex I-B172, CI-B172, CIB172, NADH-ubiquinone oxidoreductase subunit B172, NDUFA12, DAP13
Tested Applications
WB
Physical Properties
Liquid

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