Gene: CHMP2B
Official Full Name: charged multivesicular body protein 2Bprovided by HGNC
Gene Summary: This gene encodes a component of the heteromeric ESCRT-III complex (Endosomal Sorting Complex Required for Transport III) that functions in the recycling or degradation of cell surface receptors. ESCRT-III functions in the concentration and invagination of ubiquitinated endosomal cargos into intralumenal vesicles. The protein encoded by this gene is found as a monomer in the cytosol or as an oligomer in ESCRT-III complexes on endosomal membranes. It is expressed in neurons of all major regions of the brain. Mutations in this gene result in one form of familial frontotemporal lobar degeneration. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO28543 | CHMP2B Knockout cell line (HeLa) | Human | CHMP2B | 1:3~1:6 | Negative | Online Inquiry |
KO28544 | CHMP2B Knockout cell line (HCT 116) | Human | CHMP2B | 1:2~1:4 | Negative | Online Inquiry |
KO28545 | CHMP2B Knockout cell line (HEK293) | Human | CHMP2B | 1:3~1:6 | Negative | Online Inquiry |
KO28546 | CHMP2B Knockout cell line (A549) | Human | CHMP2B | 1:3~1:4 | Negative | Online Inquiry |
CHMP2B Gene Knockout Cell Lines are specifically engineered cellular models that allow for the robust study of the CHMP2B gene, which plays a crucial role in the endosomal sorting complex required for transport (ESCRT) machinery. These cell lines are generated through advanced CRISPR-Cas9 gene editing technology, resulting in a precise knockout of the CHMP2B gene, enabling researchers to investigate its function and related pathways with enhanced clarity.
The primary function of these knockout cell lines is to provide a platform for exploring the biological implications of CHMP2B loss in cellular processes, particularly those associated with neurodegenerative diseases like frontotemporal dementia. By observing the phenotypic changes, researchers can elucidate the mechanisms through which CHMP2B disruption affects cellular homeostasis and protein degradation pathways, thereby offering insights into potential therapeutic targets.
The scientific significance of CHMP2B Gene Knockout Cell Lines is profound, especially in translational research where understanding the molecular underpinnings of neurodegeneration is imperative. These cell lines are invaluable for drug discovery efforts, allowing for the screening of pharmacological agents that might restore function or compensate for the genetic loss. In clinical settings, they serve as models for better understanding patient-specific disease mechanisms, thereby accelerating the development of personalized medicine approaches.
What sets our CHMP2B Gene Knockout Cell Lines apart from conventional cellular models is their high fidelity in mimicking disease phenotypes, coupled with the ease of use in various experimental setups. Unlike traditional knockdown techniques, which can result in incomplete gene inhibition, our knockout models provide a complete absence of the CHMP2B protein, ensuring that the researchers are working with the most relevant biological information.
Our commitment to providing cutting-edge tools in molecular and cellular biology is backed by years of expertise in genetic engineering and a portfolio of high-quality biological products. With CHMP2B Gene Knockout Cell Lines, researchers and clinicians gain an essential resource that will not only advance their projects but also contribute to our collective understanding of complex diseases, ultimately fostering innovations in therapeutic strategies.
Please note that all services are for research use only. Not intended for any clinical use.
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