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抗Human ATP5O 抗体:
抗Mouse (Murine) ATP5O 抗体:
抗Rat (Rattus) ATP5O 抗体:
Upon IF1 (显示 ATPIF1 抗体) interaction with the ATP synthase both the synthetic and hydrolytic activities of the engine of oxidative phosphorylation are inhibited. (Review)
Sirt3 (显示 SIRT3 抗体) physically interacted with the OSCP and led to its subsequent deacetylation.
Genetic variation and age are associated with skeletal muscle ATP5O mRNA expression and glucose disposal rate, suggesting that combinations of genetic and non-genetic factors may cause the reduced expression of ATP5O in type 2 diabetes muscle
Nuclear magnetic resonance characterisation of the interaction between OSCP-N terminal and a peptide corresponding to residues 1-25 of the alpha-subunit (显示 POLG 抗体) of bovine F(1)-ATPase (显示 DNAH8 抗体), is presented.
The protein encoded by this gene is a component of the F-type ATPase found in the mitochondrial matrix. F-type ATPases are composed of a catalytic core and a membrane proton channel. The encoded protein appears to be part of the connector linking these two components and may be involved in transmission of conformational changes or proton conductance.
ATP synthase subunit O, mitochondrial
, human ATP synthase OSCP subunit
, oligomycin sensitivity conferral protein
, oligomycin sensitivity conferring protein
, ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit (oligomycin sensitivity conferring protein)
, ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit; DNA segment, Chr 12, Wayne State University 28, expressed
, Oligomycin sensitivity conferral protein
, mitochondrial ATP5O
, sperm flagella protein 4
, mitochondrial ATP synthase, O subunit
, mitochondrial ATP synthase O subunit
, ATP synthase oligomycin sensitivity conferral protein
, un-named hi3619
, unm hi3619