Gene: ATP8B2
Official Full Name: ATPase phospholipid transporting 8B2provided by HGNC
Gene Summary: The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO19566 | ATP8B2 Knockout cell line (HeLa) | Human | ATP8B2 | 1:3~1:6 | Negative | Online Inquiry |
KO19567 | ATP8B2 Knockout cell line (HCT 116) | Human | ATP8B2 | 1:2~1:4 | Negative | Online Inquiry |
KO19568 | ATP8B2 Knockout cell line (HEK293) | Human | ATP8B2 | 1:3~1:6 | Negative | Online Inquiry |
KO19569 | ATP8B2 Knockout cell line (A549) | Human | ATP8B2 | 1:3~1:4 | Negative | Online Inquiry |
ATP8B2 Gene Knockout Cell Lines are precisely engineered cellular models that lack functional ATP8B2 gene expression, which encodes a member of the P-type ATPase family involved in cellular lipid transport and homeostasis. These knockout cell lines serve as vital tools for investigating the biological roles of ATP8B2, particularly in context to its implications in conditions such as progressive familial intrahepatic cholestasis and other hepatic disorders.
The primary mechanism underpinning the functionality of these cell lines lies in their ability to replicate the loss-of-function mutation characteristic of ATP8B2 knockout models. This enables researchers to explore the resultant phenotypic and molecular changes, such as altered lipid profiles, dysregulated cholesterol transport, and enhanced susceptibility to cholestatic injury. By using these models, scientists can dissect the pathway disruptions caused by the absence of ATP8B2 and develop targeted therapeutic strategies.
The scientific importance of ATP8B2 Gene Knockout Cell Lines is underscored by their applications in both fundamental research and clinical settings. They are essential for drug discovery processes, particularly in evaluating potential treatments for liver diseases associated with ATP8B2 dysfunction. Additionally, their use in translational research can facilitate quality elucidation of disease mechanisms, contributing to the advancement of precision medicine.
Compared to alternative models, our ATP8B2 Gene Knockout Cell Lines are characterized by their high specificity and reproducibility, robust characterization, and user-friendly handling. Unlike many traditional gene knockout approaches, these engineered lines save time and resources by providing consistent results and enabling rapid experimentation, thus streamlining the research process.
For researchers, clinicians, and biotechnology companies alike, the value of ATP8B2 Gene Knockout Cell Lines lies in their capability to bridge gaps in understanding the complex pathophysiology associated with ATP8B2-related diseases. By integrating these models into research pipelines, users can advance their insights and facilitate the development of innovative therapeutics.
Our company, with its robust track record of generating high-quality biological products and cutting-edge genetic engineering, is committed to providing exceptional research tools such as the ATP8B2 Gene Knockout Cell Lines, designed to meet the evolving needs of the scientific community.
Please note that all services are for research use only. Not intended for any clinical use.
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