Gene: APOL1
Official Full Name: apolipoprotein L1provided by HGNC
Gene Summary: This gene encodes a secreted high density lipoprotein which binds to apolipoprotein A-I. Apolipoprotein A-I is a relatively abundant plasma protein and is the major apoprotein of HDL. It is involved in the formation of most cholesteryl esters in plasma and also promotes efflux of cholesterol from cells. This apolipoprotein L family member may play a role in lipid exchange and transport throughout the body, as well as in reverse cholesterol transport from peripheral cells to the liver. Several different transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO34056 | APOL1 Knockout cell line (A549) | Human | APOL1 | 1:3~1:4 | Negative | Online Inquiry |
APOL1 Gene Knockout Cell Lines are specifically engineered cellular models designed to lack the expression of the Apolipoprotein L1 (APOL1) gene, which is integral to studying genetic contributions to kidney diseases, particularly in populations of African descent. This product facilitates investigations into the role of APOL1 variants in the development of renal pathologies, such as focal segmental glomerulosclerosis (FSGS) and hypertension-associated nephropathy.
The key function of these knockout cell lines lies in their ability to provide a controlled environment for examining the downstream effects of APOL1 inactivity, enabling researchers to dissect the pathways through which APOL1 alleles influence cell survival, apoptosis, and inflammation. The knockout mechanism is accomplished through targeted gene editing techniques, such as CRISPR-Cas9, ensuring precision in gene disruption, thereby providing reliable and reproducible experimental models.
The scientific importance of APOL1 Gene Knockout Cell Lines is profound, as they represent a crucial tool for investigating the molecular underpinnings of cardiovascular and renal diseases. They are invaluable in both basic research and translational applications, simplifying the process of drug discovery and elucidating therapeutic targets. Furthermore, these models can be employed in various preclinical studies to assess the efficacy and safety of novel therapeutics aimed at mitigating APOL1-related pathologies.
Compared to alternative models, which may include wild-type or non-targeted cell lines, APOL1 Gene Knockout Cell Lines offer significant advantages. They provide enhanced specificity for APOL1-related studies, reducing the noise associated with background gene expression. Their streamlined application in experiments enhances the reproducibility of results and accelerates the research timeline.
For researchers and clinicians focused on gene-related diseases, these cell lines represent a highly valuable asset, providing cutting-edge insights that could lead to innovative solutions in disease management. By leveraging our expertise in genetic engineering and a robust understanding of biological pathways, our company is committed to delivering high-quality products that further scientific discovery and clinical advancement.
Please note that all services are for research use only. Not intended for any clinical use.
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