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BEST1 Knockout Cell Lines

Gene: BEST1

Official Full Name: bestrophin 1provided by HGNC

Gene Summary: This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO34824 BEST1 Knockout cell line (HeLa) Human BEST1 1:3~1:6 Negative Online Inquiry
KO34825 BEST1 Knockout cell line (HCT 116) Human BEST1 1:2~1:4 Negative Online Inquiry
KO34826 BEST1 Knockout cell line (A549) Human BEST1 1:3~1:4 Negative Online Inquiry

Background

BEST1 Gene Knockout Cell Lines are specifically engineered cellular models that lack the expression of the BEST1 gene, providing a crucial tool for studying the physiological and pathological roles of this gene. BEST1, known as Bestrophin-1, encodes a calcium-activated chloride channel that is essential for retinal health and is implicated in various diseases, including Best disease. These knockout cell lines facilitate the examination of gene function through the elimination of BEST1's activity, allowing researchers to observe resultant changes in cellular behavior and signaling pathways.

The key function of the BEST1 Gene Knockout Cell Lines involves their ability to mimic the effects of genetic mutations observed in diseases linked to the BEST1 gene. By comparing these lines with wild-type counterparts, scientists can dissect the downstream effects of loss-of-function mutations, analyzing alterations in ion channel activity, cellular excitability, and potential interactions with other cellular proteins. This mechanistic insight is critical in elucidating the pathophysiology of associated disorders.

Scientifically, the availability of BEST1 Gene Knockout Cell Lines represents a significant advancement in biomedical research and therapeutic studies. They are invaluable in the exploration of gene therapy approaches for retinal disorders and provide a platform for drug screening. In clinical settings, these models enhance our understanding of the molecular underpinnings of diseases, potentially guiding the development of targeted interventions.

Compared to alternative knockout models, the BEST1 Gene Knockout Cell Lines offer several advantages, including higher specificity in the disruption of the target gene, robust characterization of cellular responses, and the reproducibility necessary for validation across multiple studies. Their well-defined genetic background ensures consistency in experimental results, marking them as a superior choice for investigative purposes.

For researchers and clinicians, these cell lines represent not only an opportunity to advance knowledge in retinal diseases but also a pathway to discovering novel therapeutic targets. By utilizing BEST1 Gene Knockout Cell Lines, experts can innovate treatments that may eventually lead to improved patient outcomes.

Our company prides itself on advancing the field of molecular biology with high-quality, rigorously validated biological products. With a commitment to excellence and a portfolio of premier cell lines, we empower researchers to push the boundaries of scientific discovery.

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

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