Recombinant Zebrafish ATXN7L2A

• Cat.No.: ATXN7L2A-4278Z
• Product Overview: Recombinant Zebrafish ATXN7L2A full length or partial length protein was expressed.

Specification

• Source: Mammalian Cells
• Species: Zebrafish
• 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: atxn7l2a ataxin 7-like 2a [ Danio rerio (zebrafish) ]
• Official Symbol: ATXN7L2A
• Gene ID: 692316
• mRNA Refseq: NM_001045285
• Protein Refseq: NP_001038750
• UniProt ID: Q1JPV4

Reviews

07/18/2019

The ability of manufacturers to tailor products to meet specific customer needs is an added advantage, providing tailored solutions for each application.

04/10/2019

Manufacturer's products are designed to promote sustainability, minimal waste and maximum efficiency.

03/31/2019

ATXN7L2A is a good choice for Western-blot analysis due to its strong band and specificity.

Q&As

What is the structural feature of ATXN7L2A protein?

The ATXN7L2A protein contains multiple domains, including an N-terminal domain and a C-terminal domain. Its domains can interact with other proteins and thus participate in different cellular processes.

What is the significance of ATXN7L2A protein research?

It helps to understand its mechanism of action in gene regulation and its relationship with the occurrence and development of diseases. This will help us to better understand the mechanism of diseases, and provide new ideas and methods for the prevention and treatment of related diseases.

What is the regulatory mechanism of ATXN7L2A protein?

The expression of ATXN7L2A protein is affected by a variety of regulatory mechanisms, including transcriptional level regulation, post-transcriptional modification and protein degradation. These mechanisms can affect the abundance and activity of ATXN7L2A protein in cells.

Is ATXN7L2A associated with disease?

ATXN7L2A protein is associated with many diseases, including nervous system diseases, cancer and metabolic disorders. For example, mutations in the ATXN7L2A protein are associated with genetic disorders such as Speller's syndrome.

What is the status of ATXN7L2A protein?

The study of ATXN7L2A protein is still in its early stage, and the understanding of its function and regulatory mechanism is still needed. However, several studies have identified disease mutations associated with the ATXN7L2A protein and attempted through cellular and animal models

How do defects in ATXN7L2A affect cells and organisms?

Defective ATXN7L2A protein function may lead to the disorder of transcriptional regulation, which in turn affects the normal function of cells. This may lead to abnormalities in cell proliferation, differentiation, apoptosis and other processes, thereby affecting the physiological and pathological processes of the organism.