Home  >  Products  >  Atp5c1 (Atp5c1 ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 ) Blocking Peptide (the N terminal of Atp5c1)(100ug)
Atp5c1 (Atp5c1 ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 ) Blocking Peptide (the N terminal of Atp5c1)(100ug)

Atp5c1 (Atp5c1 ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 ) Blocking Peptide (the N terminal of Atp5c1)(100ug)


Supplier: Aviva Systems Biology Incorporated
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This is a synthetic peptide designed for use in combination with anti-Atp5c1 Antibody (ARP48275_P050), made by Aviva Systems Biology. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
Reactivities: Human, Mouse
Presku: AAP48275
Size: 100ug
Weight: 30kDa
Gene: 11949
Format: Lyophilized powder
Target: Mitochondrial membrane ATP synthase (F1F0 ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F1 - containing the extramembraneous catalytic core, and F0 - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F1 is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Part of the complex F1 domain and the central stalk which is part of the complex rotary element. The gamma subunit protrudes into the catalytic domain formed of alpha3beta3. Rotation of the central stalk against the surrounding alpha3beta3 subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits.
Alternative names: 1700094F02Rik