Overview |
bsm-54649R |
NDUFAF1 Monoclonal Antibody |
WB, FCM, IHC-P, IF(ICC), IHC |
Human |
Specifications |
Unconjugated |
Rabbit |
Synthetic Peptide within C terminal human NDUFAF1. |
Monoclonal |
13C5 |
IgG |
1ug/ul |
Purified by Protein A. |
Aqueous buffered solution containing 1xTBS (pH7.4), 1%BSA, 40%Glycerol and 0.05% Sodium Azide. |
Store at -20°C for 12 months. |
Target |
51103 |
Q9Y375 |
Mitochondrion |
CGI 65 antibody, CGI65 antibody, CIA30 antibody, CIA30_HUMAN antibody, Complex I intermediate associated protein 30 antibody, Complex I intermediate associated protein 30 mitochondrial antibody, Complex I intermediate-associated protein 30, mitochondrial antibody, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 1 antibody, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 1 antibody, NADH:ubiquinone oxidoreductase complex assembly factor 1 antibody, NDUFAF 1 antibody, Ndufaf1 antibod |
This gene encodes a complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) 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. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Dec 2011] |
Application Dilution |
WB |
1:300-5000 |
FCM |
1:20-100 |
IHC-P |
1:200-400 |
IF(ICC) |
1:50-200 |
IHC |
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