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Invitrogen™ NDUFA12 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA596981
Description
Immunogen sequence: MELVQVLKRG LQQITGHGGL RGYLRVFFRT NDAKVGTLVG EDKYGNKYYE DNKQFFGRHR WVVYTTEMNG KNTFWDVDGS MVPPEWHRWL HSMTDDPPTT KPLTARKFIW TNHKFNVTGT PEQYVPYSTT RKKIQEWIPP STPYK; Positive Samples: 293T, PC-12, HepG2, Mouse kidney, Mouse heart, Mouse testis, Rat heart, Rat brain; Cellular Location: Matrix side, Mitochondrion inner membrane, Peripheral membrane protein.
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.
Specifications
NDUFA12 | |
Polyclonal | |
Unconjugated | |
Ndufa12 | |
13 kDa differentiation-associated protein; 13kDa differentiation-associated protein; 2410011G03Rik; AW112974; B17.2; CIB17.2; CI-B17.2; complex I B17.2 subunit; complex I-B17.2; DAP13; DAP13 protein; hypothetical protein LOC613140; NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12; NADH:ubiquinone oxidoreductase b17.2 subunit; NADH:ubiquinone oxidoreductase subunit A12; NADH-ubiquinone oxidoreductase subunit B17.2; Ndufa12; RGD1311462; si:dkey-183c16.3; zgc:112053 | |
Rabbit | |
Affinity chromatography | |
RUO | |
299739, 55967, 66414 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
ELISA, Western Blot | |
2.32 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
Q7TMF3, Q9UI09 | |
Ndufa12 | |
Recombinant fusion protein containing a sequence corresponding to amino acids 1-145 of human NDUFA12 (NP_0613261). | |
100 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
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