Recombinant Mouse RHOT1 Protein Pre-coupled Magnetic Beads

• Cat.No.: RHOT1-7592M-B
• Product Overview: The Recombnant protein was conjugated to magnetic beads. This ready-to-use, pre-coupled magnetic beads are in uniform particle size and narrow size distribution with large surface area, which is conducive to convenient and fast capture target molecules with high specificity and achieve magnetic separation. This product can be equipped with automation equipment for high-throughput operations.

Specification

• Source: HEK293
• Species: Mouse
• Form: Solution
• Particle size: ~2 μm
• Beads Surface: Hydrophilic
• Capacity: > 200 pmol rabbit IgG/ mg beads
• Applications: Immunoassay, In vitro diagnostics, cell sorting, Immunoprecipitation/Co-precipitation, Protein/antibody separation and purification.
• Stability: Stable for at least 6 months from the date of receipt of the product under proper storage and handling conditions.
• Storage: 2-8℃. Do not to freeze thaw the Beads
• Concentration: 10mg beads/mL
• Storage Buffer: PBS buffer

Gene Information

• Gene Name: Rhot1 ras homolog gene family, member T1 [ Mus musculus ]
• Official Symbol: RHOT1
• Gene ID: 59040
• mRNA Refseq: NM_001163354.1
• Protein Refseq: NP_001156826.1
• UniProt ID: Q8BG51

Reviews

08/25/2022

This versatility allows me to explore different aspects of my research with confidence and accuracy.

01/10/2020

the RHOT1 protein's excellent functionality makes it highly suitable for various trial applications.

06/17/2018

Whether I am investigating enzymatic activity, studying protein-protein interactions, or testing its role in signaling pathways, the RHOT1 protein consistently performs exceptionally well.

Q&As

Are there any specific inhibitors or activators of RHOT1 protein currently being developed for clinical use?

Researchers are exploring the development of small molecule inhibitors or activators targeting RHOT1 protein for potential clinical applications in the future.

How is the RHOT1 protein related to neurodegenerative diseases?

Dysregulation of RHOT1 protein has been implicated in neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease.

Can mutations in the RHOT1 gene lead to mitochondrial dysfunction?

Yes, mutations in the RHOT1 gene can disrupt mitochondrial dynamics and lead to mitochondrial dysfunction, which may contribute to the development of various diseases.

What are the cellular functions of RHOT1 protein?

RHOT1 protein is involved in the maintenance of mitochondrial morphology, regulation of mitochondrial fission and fusion, and control of mitochondrial dynamics.

Are there any potential therapeutic targets related to the RHOT1 protein?

RHOT1 protein and its associated pathways are being investigated as potential therapeutic targets for neurodegenerative diseases and other disorders characterized by mitochondrial dysfunction.