Recombinant Mouse ELAC1 Protein

• Cat.No.: ELAC1-5120M
• Product Overview: Recombinant Mouse ELAC1 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: Elac1 elaC homolog 1 (E. coli) [ Mus musculus ]
• Official Symbol: ELAC1
• Gene ID: 114615
• mRNA Refseq: NM_053255.3
• Protein Refseq: NP_444485.2
• UniProt ID: Q8VEB6

Reviews

03/07/2018

The ELAC1 Protein exhibits remarkable stability and functionality, making it an optimal choice for a wide range of applications in various fields.

10/31/2017

Its exceptional purity and consistency have consistently yielded reliable and reproducible results, ensuring the accuracy and reliability of my research outcomes.

07/10/2016

Their prompt and knowledgeable assistance has been instrumental in overcoming hurdles and has significantly contributed to the success of my research.

Q&As

How is ELAC1 protein relevant to mitochondrial disorders?

ELAC1 protein is involved in maintaining mitochondrial function, and mutations in the ELAC1 gene can contribute to mitochondrial disorders.

Are there any clinical trials focusing on ELAC1 protein for mitochondrial disorders?

Clinical trials investigating the role of ELAC1 protein in mitochondrial disorders are currently underway, aiming to develop targeted therapies.

Are there any specific treatments targeting ELAC1 protein for mitochondrial disorders?

As of now, there are no specific treatments targeting ELAC1 protein for mitochondrial disorders, but ongoing research may lead to future therapeutic approaches.

What other diseases are associated with mutations in ELAC1 gene?

In addition to pontocerebellar hypoplasia and mitochondrial disorders, mutations in ELAC1 gene have been linked to infantile hypertrophic cardiomyopathy.

How does ELAC1 protein affect cardiac function?

ELAC1 protein plays a role in mitochondrial RNA processing, which is essential for proper cardiac function. Mutations in ELAC1 gene can lead to cardiomyopathy.