Gene: ATP8B1
Official Full Name: ATPase phospholipid transporting 8B1provided by HGNC
Gene Summary: This gene encodes a member of the P-type cation transport ATPase family, which belongs to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. Mutations in this gene may result in progressive familial intrahepatic cholestasis type 1 and in benign recurrent intrahepatic cholestasis. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03230 | ATP8B1 Knockout cell line (HeLa) | Human | ATP8B1 | 1:3~1:6 | Negative | Online Inquiry |
KO03231 | ATP8B1 Knockout cell line (HCT 116) | Human | ATP8B1 | 1:2~1:4 | Negative | Online Inquiry |
KO03232 | ATP8B1 Knockout cell line (HEK293) | Human | ATP8B1 | 1:3~1:6 | Negative | Online Inquiry |
KO03233 | ATP8B1 Knockout cell line (A549) | Human | ATP8B1 | 1:3~1:4 | Negative | Online Inquiry |
ATP8B1 Gene Knockout Cell Lines are genetically engineered cell lines that have undergone specific editing to deactivate the ATP8B1 gene, which plays a crucial role in phospholipid transport and is implicated in various biological processes, including bile salt secretion and lipid metabolism. By creating these knockout models, researchers can study the functional consequences of ATP8B1 deficiency, thereby gaining insights into neurodegenerative diseases, cholesterol metabolism disorders, and liver functions.
The primary mechanism by which ATP8B1 Gene Knockout Cell Lines operate involves a significant alteration in cellular lipid composition, leading to dysregulated transport processes and accumulation of specific phospholipid species. This provides a platform to investigate the downstream effects on cell signaling, metabolic pathways, and cellular stress responses associated with ATP8B1 deficiency. Researchers can utilize these models in experiments aimed at elucidating the pathophysiology of related diseases and testing therapeutic interventions.
The scientific importance of these cell lines is tremendous, particularly in the context of drug discovery and development. They enable precise exploration of disease mechanisms and facilitate the identification of potential pharmaceutical targets, thereby propelling forward the quest for innovative treatment strategies. Furthermore, these knockout cell lines serve as vital tools for phenotypic screening, allowing for the evaluation of compound efficacy and safety within a controlled genetic background.
What sets ATP8B1 Gene Knockout Cell Lines apart from alternative models is their specificity and relevance to human physiology. Unlike general genetic models, these lines provide a focused assessment of ATP8B1’s role in cellular processes, ensuring results are more translatable to clinical scenarios. Researchers and clinicians can leverage these unique attributes to advance their studies in an efficiently time-effective manner.
With a commitment to advancing biological research, our company specializes in providing high-quality genetic models like the ATP8B1 Gene Knockout Cell Lines. By combining cutting-edge technology with expert knowledge, we ensure robust research outcomes that can pave the way for breakthroughs in healthcare and related fields.
Please note that all services are for research use only. Not intended for any clinical use.
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.
There is no product in your cart. |
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.