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BAX Knockout Cell Lines

Gene: BAX

Official Full Name: BCL2 associated X, apoptosis regulatorprovided by HGNC

Gene Summary: The protein encoded by this gene belongs to the BCL2 protein family. BCL2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. This protein forms a heterodimer with BCL2, and functions as an apoptotic activator. The association and the ratio of BAX to BCL2 also determines survival or death of a cell following an apoptotic stimulus. This protein is reported to interact with, and increase the opening of, the mitochondrial voltage-dependent anion channel (VDAC), which leads to the loss in membrane potential and the release of cytochrome c. The expression of this gene is regulated by the tumor suppressor P53 and has been shown to be involved in P53-mediated apoptosis. Multiple alternatively spliced transcript variants, which encode different isoforms, have been reported for this gene. [provided by RefSeq, Dec 2019]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO07627 BAX Knockout cell line (HeLa) Human BAX 1:3~1:6 Negative Online Inquiry
KO07628 BAX Knockout cell line (HCT 116) Human BAX 1:2~1:4 Negative Online Inquiry
KO07629 BAX Knockout cell line (HEK293) Human BAX 1:3~1:6 Negative Online Inquiry
KO07630 BAX Knockout cell line (A549) Human BAX 1:3~1:4 Negative Online Inquiry

Background

BAX Gene Knockout Cell Lines are genetically engineered cell lines designed specifically to eliminate the expression of the BAX gene, which is widely known for its role in promoting apoptosis, or programmed cell death. This product provides a critical tool for researchers aiming to study cell survival, signaling pathways, and the mechanisms underlying various diseases characterized by dysregulated apoptosis, including cancer. By knocking out the BAX gene, these cell lines allow scientists to explore alternative survival pathways and assess the cellular response to stress without the influence of BAX-mediated apoptotic processes.

These cell lines operate through a precise gene editing technique, typically employing CRISPR-Cas9 technology, to disrupt the BAX gene's coding sequence. The resulting phenotypic changes can be accurately studied to understand the cellular mechanisms involved in anti-apoptotic responses, enabling researchers to identify potential therapeutic targets for cancer treatments and other apoptosis-related conditions. The elimination of BAX provides a controlled environment to study cellular responses to various stimuli, such as chemotherapeutic agents or environmental stressors, leading to valuable insights in both basic and applied biomedical research.

The scientific importance of BAX Gene Knockout Cell Lines extends to their application in both basic research and clinical settings, including drug discovery, cancer biology studies, and the validation of new therapeutic approaches. They are particularly useful in high-throughput screening assays, allowing researchers to test large libraries of compounds in a consistent and reproducible environment.

Compared to alternative cell lines with partial gene knockdowns or wild-type versions, BAX Gene Knockout Cell Lines offer a complete loss of function, providing a more definitive platform for exploring the cellular pathways involved in cell death and survival. This unique advantage can lead to more robust data and clearer insights into the roles of apoptosis in various biological contexts.

For researchers and clinicians, the value of BAX Gene Knockout Cell Lines lies in their ability to facilitate innovative research, therapeutic development, and the potential to identify novel treatments for diseases associated with apoptosis dysregulation. Our company specializes in producing high-quality genetic tools, and our expertise ensures that our cell lines are validated and meet rigorous standards, making them a reliable choice for advancing your research objectives.

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

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