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ABCB8 Knockout Cell Lines

Gene: ABCB8

Official Full Name: ATP binding cassette subfamily B member 8provided by HGNC

Gene Summary: This nuclear gene encodes a multi-pass membrane protein that is targeted to the mitochondrial inner membrane. The encoded protein is an ATP-dependent transporter that may mediate the passage of organic and inorganic molecules out of the mitochondria. Loss of function of the related gene in mouse results in a disruption of iron homeostasis between the mitochondria and cytosol. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO31093 ABCB8 Knockout cell line (HeLa) Human ABCB8 1:3~1:6 Negative Online Inquiry
KO31094 ABCB8 Knockout cell line (HCT 116) Human ABCB8 1:2~1:4 Negative Online Inquiry
KO31095 ABCB8 Knockout cell line (HEK293) Human ABCB8 1:3~1:6 Negative Online Inquiry
KO31096 ABCB8 Knockout cell line (A549) Human ABCB8 1:3~1:4 Negative Online Inquiry

Background

ABCB8 Gene Knockout Cell Lines are genetically engineered cell models specifically designed to lack the ATP-binding cassette sub-family B member 8 (ABCB8) gene. ABCB8 is known for its role in mitochondrial function, particularly in the transport of metabolites and maintenance of mitochondrial integrity. These knockout cell lines serve as essential tools for studying the physiological and pathological roles of ABCB8, providing insights into diseases such as cancer, neurodegenerative disorders, and metabolic syndromes.

The principal function of these knockout cell lines is to facilitate the investigation of the gene's impact on cellular processes, particularly with respect to mitochondrial bioenergetics and apoptotic pathways. By eliminating ABCB8 expression, researchers can assess changes in mitochondrial morphology, reactive oxygen species production, and cellular metabolism. This unobstructed experimental setup enables researchers to delineate the direct consequences of ABCB8 deficiency on cell survival and function, enhancing our understanding of various health conditions linked to mitochondrial dysfunction.

Scientific applications of ABCB8 Gene Knockout Cell Lines are vast, ranging from drug discovery and toxicity testing to elucidating mechanisms behind disease progression. In clinical settings, these cell lines can serve as models for evaluating therapeutic interventions aimed at restoring normal mitochondrial function in affected tissues.

What sets our ABCB8 Gene Knockout Cell Lines apart from alternatives is their exceptional genetic fidelity and robust performance across varied experimental conditions. Our lines are meticulously validated to ensure complete knockout efficacy and the absence of functional compensation by other ATP-binding cassette transporters. This specificity enhances the reliability of experimental outcomes, making them indispensable for cutting-edge research.

For researchers and clinicians, investing in ABCB8 Gene Knockout Cell Lines is invaluable, opening avenues for innovative research while providing a platform for potential therapeutic development. Our deep expertise in genetic engineering and commitment to quality ensures that you receive the highest standard of biological products to advance your research goals.

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

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