Recombinant Mouse ATXN7 Protein

• Cat.No.: ATXN7-2198M
• Product Overview: Recombinant Mouse ATXN7 full length or partial length protein was expressed.

Specification

• Source: Mammalian Cells
• Species: Mouse
• Tag: His
• Form: Liquid or lyophilized powder
• Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method.
• Purity: >80%
• Notes: This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications.
• Storage: Store it at +4 ºC for short term. For long term storage, store it at -20 ºC～-80 ºC.
• Storage Buffer: PBS buffer

Gene Information

• Gene Name: Atxn7 ataxin 7 [ Mus musculus ]
• Official Symbol: ATXN7
• Gene ID: 246103
• mRNA Refseq: NM_139227.4
• Protein Refseq: NP_631973.3
• UniProt ID: Q8R4I1

Reviews

04/26/2022

Because the extraordinary stability of ATXN7 under various conditions highlights its robustness and versatility.

02/03/2021

Application range of ATXN7 is really wide, from the laboratory to the clinic, can see its figure, it is really rare.

01/27/2019

This powerful biological activity of proteins combined with their high purity makes their experimental results extremely reliable, which is of great significance in the field of scientific research.

Q&As

What are the structural features of ATXN7 protein?

The ATXN7 protein consists of multiple functional domains, including multiple HEAT repeats, which may be involved in protein interactions and regulation of function.

How about the cellular localization of ATXN7 protein?

ATXN7 protein is mainly located in the nucleus and participates in the regulation of gene transcription.

What is the regulatory mechanism of ATXN7 protein?

The expression and function of ATXN7 protein are affected by multiple regulatory mechanisms, including transcriptional regulation, post-translational modification, and protein-protein interaction.

What are the implications of ATXN7 protein research for disease treatment?

In-depth study of the function and regulatory mechanism of ATXN7 protein will help to reveal the mechanism of spinocerebellar ataxia (SCA7) and provide new targets and strategies for the diagnosis and treatment of the disease.

Which diseases are associated with ATXN7 protein mutations?

The protein mutations are associated with the development of spinocerebellar ataxia (SCA7).

How does the ATXN7 protein interact with other proteins?

ATXN7 protein interacts with multiple proteins, including transcription factors, coactivators, and other regulatory proteins.