Recombinant Mouse Atp5e Protein, Myc/DDK-tagged

• Cat.No.: Atp5e-1769M
• Product Overview: Purified recombinant protein of mouse full-length ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit (Atp5e), with C-terminal MYC/DDK tag, expressed in HEK293T cells.

Specification

• Description: 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 of the central stalk which is part of the complex rotary element. Rotation of the central stalk against the surrounding alpha3beta3 subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits.
• Source: HEK293T
• Species: Mouse
• Tag: Myc&DDK
• Molecular Mass: 5.8 kDa
• Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining
• Stability: Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
• Storage: Store at -80 centigrade after receiving vials.
• Concentration: >50 μg/mL as determined by microplate BCA method
• Storage Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.

Gene Information

• Gene Name: Atp5e ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit [ Mus musculus (house mouse) ]
• Official Symbol: Atp5e
• Synonyms: ATP5E; ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit; ATP synthase subunit epsilon, mitochondrial; ATPase subunit epsilon; ATP synthase epsilon chain, mitochondrial; ATPE; AV000645; 2410043G19Rik
• Gene ID: 67126
• mRNA Refseq: NM_025983
• Protein Refseq: NP_080259
• UniProt ID: P56382

Reviews

09/26/2022

The manufacturer's products are derived from sustainable sources, ensuring minimal impact on the environment and local communities.

05/19/2022

This manufacturer's reputation for excellence in protein production is well deserved, with a focus on customer satisfaction and reliable delivery.

01/13/2019

Because proteins have short half-lives, they can be delivered more precisely and in a controlled manner, ensuring optimal therapeutic effects.

Q&As

What is the role of ATP5E in tumors?

ATP5E may play a role in tumor cell metabolism and energy supply.

Are ATP5E mutations associated with nervous system diseases?

Yes, ATP5E gene mutations are associated with certain neurological disorders such as Parkinson's disease, spinocerebellar ataxia, etc.

What is the role of ATP5E protein in metabolic diseases?

ATP5E protein may be associated with the occurrence and progression of metabolic diseases such as obesity and diabetes.

How are ATP5E mutations associated with disease?

Gene mutation may lead to abnormal protein structure or function, which in turn affects the physiological function of the protein and is associated with specific diseases.

What are the regulatory mechanisms of ATP5E?

ATP5E expression and function are affected by a variety of regulatory mechanisms, including regulation of transcription factors and epigenetic modifications.

In which tissues or organs is ATP5E highly expressed?

It is highly expressed in multiple tissues and organs, especially metabolically active tissues such as heart, liver, and brain.