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Recombinant Human ATP5G1, GST-tagged

Cat.No.: ATP5G1-3698H
Product Overview: ATP synthase lipid-binding protein, mitochondrial (ATP5G1)
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 the same protein have been identified.
Source: E. Coli or Yeast
Species: Human
Tag: GST
Form: This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
Protein length: 136
Purity: >90%
Notes: Small volumes of ATP5G1 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: ATP5G1 ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) [ Homo sapiens ]
Official Symbol: ATP5G1
Synonyms: ATP5G1; ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9); ATP synthase, H+ transporting, mitochondrial F0 complex, subunit c (subunit 9), isoform 1 , ATP synthase, H+ transporting, mitochondrial F0 complex, subunit C1 (subunit 9) , ATP5G; ATP synthase lipid-binding protein, mitochondrial; ATPase protein 9; ATPase subunit 9; ATPase subunit C; ATP synthase proteolipid P1; mitochondrial ATP synthase, subunit 9, isoform 1; mitochondrial ATP synthase, subunit C, isoform 1; ATP synthase, H+ transporting, mitochondrial F0 complex, subunit C1 (subunit 9); ATP synthase, H+ transporting, mitochondrial F0 complex, subunit c (subunit 9), isoform 1; ATP5A; ATP5G;
Gene ID: 516
mRNA Refseq: NM_001002027
Protein Refseq: NP_001002027
MIM: 603192
UniProt ID: P05496
Chromosome Location: 17q21.32
Pathway: Alzheimers disease, organism-specific biosystem; Alzheimers disease, conserved biosystem; Electron Transport Chain, organism-specific biosystem; F-type ATPase, eukaryotes, organism-specific biosystem; Formation of ATP by chemiosmotic coupling, organism-sp
Function: hydrogen ion transmembrane transporter activity; lipid binding; transporter activity;

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