Gene: ABCA1
Official Full Name: ATP binding cassette subfamily A member 1provided by HGNC
Gene Summary: The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in both alleles of this gene cause Tangier disease and familial high-density lipoprotein (HDL) deficiency. [provided by RefSeq, Sep 2019]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
GP00475 | ABCA1 gRNA7-gRNA8 KO plasmid | ABCA1 | $850 | |||
GP00576 | ABCA1 gRNA5-gRNA6 KO plasmid | ABCA1 | $850 | |||
GP00657 | ABCA1 gRNA1-gRNA2 KO plasmid | ABCA1 | $850 | |||
KO00756 | ABCA1 Knockout cell line (U-87 MG) | Human | ABCA1 | 1:3~1:4 | Negative | Online Inquiry |
KO00813 | ABCA1 Knockout cell line(ARPE-19) | Human | ABCA1 | 1:3~1:5 | Negative | Online Inquiry |
KO20091 | ABCA1 Knockout cell line (HeLa) | Human | ABCA1 | 1:3~1:6 | Negative | Online Inquiry |
KO20092 | ABCA1 Knockout cell line (A549) | Human | ABCA1 | 1:3~1:4 | Negative | Online Inquiry |
ABCA1 Gene Knockout Cell Lines are specialized cellular models engineered to lack the ATP-binding cassette sub-family A member 1 (ABCA1) gene, which plays a pivotal role in lipid metabolism, particularly in cholesterol efflux and high-density lipoprotein (HDL) formation. This knockout model provides researchers with a unique tool to investigate the molecular and biological functions of ABCA1 in both physiological and pathological contexts, including cardiovascular diseases, metabolic disorders, and neurodegenerative conditions.
The primary function of the ABCA1 protein is its involvement in the transport of phospholipids and cholesterol from cells to lipid-poor apolipoproteins, facilitating the formation of HDL particles. By utilizing our ABCA1 gene knockout cell lines, researchers can study the resultant alterations in lipid homeostasis, the cellular uptake of cholesterol, and the implications of ABCA1 deficiency on intracellular signaling pathways. The absence of functional ABCA1 allows for a more nuanced understanding of its role in macrophage cholesterol efflux, the prevention of foam cell formation, and the modulation of inflammation.
The scientific importance of these cell lines lies in their application for drug discovery, metabolic research, and the development of gene therapy strategies. They provide critical insight into how ABCA1 dysfunction contributes to atherosclerosis and other lipid-related diseases, thereby expediting the identification of potential therapeutic targets.
Compared to conventional cell lines, our ABCA1 gene knockout models offer enhanced specificity and relevance in studies related to cholesterol metabolism and cardiovascular health. The clear genetic background and reproducibility of our models facilitate reliable results, essential for high-quality scientific publications and translational research.
For researchers and clinicians searching for a robust model to explore the intricacies of lipid metabolism and cardiovascular disease mechanisms, our ABCA1 gene knockout cell lines represent an invaluable resource. With a commitment to excellence in biological product development, our company stands at the forefront of innovation, providing premium cell lines that empower scientific discovery and advancements in the field of metabolism and cardiovascular research.
Please note that all services are for research use only. Not intended for any clinical use.
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