Home / LIPA Knockout Cell Lines

LIPA Knockout Cell Lines

Gene: LIPA

Official Full Name: lipase A, lysosomal acid typeprovided by HGNC

Gene Summary: This gene encodes lipase A, the lysosomal acid lipase (also known as cholesterol ester hydrolase). This enzyme functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides. Mutations in this gene can result in Wolman disease and cholesteryl ester storage disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2014]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
GP00594 LIPA gRNA5-gRNA6 KO plasmid LIPA $850
KO00743 LIPA Knockout cell line (SH-SY5Y) Human LIPA 1:2-1:3 Negative Online Inquiry
KO16526 LIPA Knockout cell line (HeLa) Human LIPA 1:3~1:6 Negative Online Inquiry
KO16527 LIPA Knockout cell line (HCT 116) Human LIPA 1:2~1:4 Negative Online Inquiry
KO16528 LIPA Knockout cell line (HEK293) Human LIPA 1:3~1:6 Negative Online Inquiry
KO16529 LIPA Knockout cell line (A549) Human LIPA 1:3~1:4 Negative Online Inquiry

Background

LIPA Gene Knockout Cell Lines are specifically engineered cellular models designed to study the function of the LIPA gene, which encodes lysosomal acid lipase (LAL). This enzyme plays a critical role in lipid metabolism, particularly in the hydrolysis of triglycerides and cholesteryl esters within the lysosomes. By knocking out the LIPA gene, these cell lines allow researchers to elucidate the metabolic pathways influenced by LAL deficiency and assess the impact on cellular processes like lipid accumulation and inflammation.

The primary function of LIPA Gene Knockout Cell Lines lies in their ability to simulate lysosomal storage diseases, such as Wolman disease and Cholesteryl Ester Storage Disease (CESD), conditions marked by LAL deficiency. Researchers can study the biochemical alterations and pathophysiological mechanisms that arise from the absence of functional LAL, providing essential insights into disease progression and potential therapeutic targets.

From a scientific perspective, these cell lines are invaluable for both basic and applied research. They can be utilized to evaluate the efficacy of new lipid-lowering drugs or gene therapy strategies aimed at restoring LAL function. This research is critical, as it contributes to a deeper understanding of metabolic disorders and can lead to innovative treatments that may improve patient outcomes.

Compared to alternatives such as standard wild-type cell lines or primary human cells, LIPA Gene Knockout Cell Lines offer distinct advantages, including reproducibility and reduced variability, facilitating large-scale screening and analysis. Their specific targeting of the LIPA gene further ensures that experimental results are directly attributable to the loss of LAL function.

For researchers and clinicians working in the fields of genetics, metabolism, or drug discovery, LIPA Gene Knockout Cell Lines represent a powerful tool that enhances the ability to investigate disease mechanisms and test therapeutic interventions. By investing in this innovative product, users can significantly advance their work and contribute to the development of treatments that address critical unmet medical needs. Our company prides itself on delivering high-quality, precisely engineered biological products backed by years of expertise in molecular biology and cell line development, ensuring that you receive the most reliable tools for your research.

Please note that all services are for research use only. Not intended for any clinical use.

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.

0

There is no product in your cart.