Recombinant Rhesus Macaque LIPA Protein Pre-coupled Magnetic Beads

• Cat.No.: LIPA-2343R-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: Rhesus Macaque
• 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: LIPA lipase A, lysosomal acid, cholesterol esterase [ Macaca mulatta (Rhesus monkey) ]
• Official Symbol: LIPA
• Synonyms: LIPA; lysosomal acid lipase/cholesteryl ester hydrolase
• Gene ID: 695240
• mRNA Refseq: NM_001266346
• Protein Refseq: NP_001253275
• UniProt ID: F7EC56

Reviews

03/02/2019

Its reliable and accurate performance ensures dependable results, contributing to the advancement of scientific knowledge in various fields of study.

01/18/2018

The reliable performance of the LIPA protein in ELISA and its compatibility with protein electron microscopy structure analysis make it an excellent choice for a wide range of research studies.

03/05/2017

Their knowledgeable and responsive team assists in troubleshooting and finding solutions to any experimental challenges that may arise.

Q&As

How does LIPA protein deficiency affect lipid metabolism?

LIPA protein deficiency impairs the breakdown of cholesterol esters and triglycerides, leading to their accumulation in various tissues and organs.

How is LIPA protein deficiency diagnosed?

Diagnosis of LIPA protein deficiency is typically made through genetic testing and measurement of LIPA enzyme activity in blood samples.

Are there any specific dietary recommendations for individuals with LIPA protein deficiency?

Patients with LIPA protein deficiency are often advised to follow a low-fat, high-carbohydrate diet to help manage their lipid levels.

How does LIPA protein deficiency affect the liver?

LIPA protein deficiency can result in the accumulation of cholesterol esters and triglycerides in the liver, leading to liver damage and dysfunction.

Are there any ongoing research efforts focused on LIPA protein and its clinical applications?

Yes, researchers are actively studying LIPA protein deficiency and potential therapeutic approaches, including gene therapy and novel enzyme replacement strategies.