Recombinant Human ATP5G3, GST-tagged

Cat.No. : ATP5G3-3702H
Product Overview : ATP synthase lipid-binding protein, mitochondrial (ATP5G3)
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Species : Human
Source : E.Coli/Yeast
Tag : GST
Protein Length : 142
Description : This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding different proteins have been identified.
Form : This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
Purity : >90%
Notes : Small volumes of ATP5G3 recombinant protein may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice.
Storage : Store at -20 degree C. For extended storage, store at -20 or -80 degree C.
Storage Buffer : PBS pH 7.4, 50% glycerol
Warning : This product is for research use only. Not for use in diagnostic or therapeutic procedures.
Gene Name ATP5G3 ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C3 (subunit 9) [ Homo sapiens ]
Official Symbol ATP5G3
Synonyms P3
Gene ID 518
mRNA Refseq NM_001689.4
Protein Refseq NP_001680.1
MIM 602736
UniProt ID P48201
Chromosome Location 2q31.1
Pathway Alzheimers disease, organism-specific biosystem;Alzheimers disease, conserved biosystem;Electron Transport Chain, organism-specific biosystem;F-type ATPase, eukaryotes, organism-specific biosystem;Huntingtons disease, organism-specific biosystem;Huntingto
Function hydrogen ion transmembrane transporter activity;lipid binding;transporter activity;

Not For Human Consumption!

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