Recombinant Human ATP5L, His-tagged

• Cat.No.: ATP5L-3721H
• Product Overview: ATP synthase subunit g, mitochondrial (ATP5L)

Specification

• Species: Human
• Source: E.Coli/Yeast
• Tag: His
• Protein Length: 103
• Description: Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the g subunit of the Fo complex. Alternative splicing results in multiple transcript variants.
• 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 ATP5L 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 Information

• Gene Name: ATP5L
• Official Symbol: ATP5L
• Synonyms: ATP5L ; ATP5L; ATP5L; ATP5JG; ATPase sub...
• Gene ID: 10632
• mRNA Refseq: NM_006476.4
• Protein Refseq: NP_006467.4
• UniProt ID: O75964
• Chromosome Location: Chromosome: 11; NC_000011.9 (118272104..118280562). Location: 11q23.3
• Function: Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation