Gene: VIM
Official Full Name: vimentinprovided by HGNC
Gene Summary: This gene encodes a type III intermediate filament protein. Intermediate filaments, along with microtubules and actin microfilaments, make up the cytoskeleton. The encoded protein is responsible for maintaining cell shape and integrity of the cytoplasm, and stabilizing cytoskeletal interactions. This protein is involved in neuritogenesis and cholesterol transport and functions as an organizer of a number of other critical proteins involved in cell attachment, migration, and signaling. Bacterial and viral pathogens have been shown to attach to this protein on the host cell surface. Mutations in this gene are associated with congenital cataracts in human patients. [provided by RefSeq, Aug 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO01374 | VIM Knockout cell line (HeLa) | Human | VIM | 1:3~1:6 | Negative | Online Inquiry |
KO03422 | VIM Knockout cell line (HCT 116) | Human | VIM | 1:2~1:4 | Negative | Online Inquiry |
KO03423 | VIM Knockout cell line (HEK293) | Human | VIM | 1:3~1:6 | Negative | Online Inquiry |
KO03424 | VIM Knockout cell line (A549) | Human | VIM | 1:3~1:4 | Negative | Online Inquiry |
VIM Gene Knockout Cell Lines are specialized cellular models whereby the vimentin gene (VIM) has been deliberately disrupted or knocked out. Vimentin is a crucial intermediate filament protein that plays multifaceted roles in maintaining cellular structure, facilitating cell motility, and regulating various cellular processes including apoptosis and signaling pathways. By utilizing these cell lines, researchers can investigate the specific contributions of vimentin in cellular functions and its implications in pathological conditions like cancer metastasis and fibrosis.
These knockout cell lines operate through the use of CRISPR-Cas9 technology, a powerful tool for targeted gene editing that allows for precise modifications to the genomic DNA. By generating VIM-deficient cell lines, it becomes possible to explore the biochemical pathways influenced by vimentin and assess how its absence affects cellular behavior, morphology, and response to therapeutic agents. Such investigations are essential for elucidating the molecular mechanisms underlying diseases where vimentin is a critical player.
The scientific importance of VIM Gene Knockout Cell Lines lies in their utility for both basic and translational research. In clinical settings, these models can facilitate the development of targeted therapies for conditions characterized by abnormal vimentin function. Furthermore, they provide valuable insights into the mechanistic basis of tissue repair and regeneration.
Compared to alternative models, such as wild-type cell lines or those using pharmacological inhibitors, VIM Gene Knockout Cell Lines offer a clean genetic background for studying vimentin's role without the confounding effects of incomplete inhibition. This specificity allows for more reliable conclusions regarding vimentin's contributions to various cellular processes.
For researchers and clinicians alike, the value of VIM Gene Knockout Cell Lines lies in their ability to provide a controlled platform for more nuanced investigations, enabling advancements in disease understanding and the formulation of novel treatment strategies. At [Your Company Name], our expertise in cell line generation and genetic engineering ensures high-quality, reproducible products that empower the scientific community to break new ground in research.
Please note that all services are for research use only. Not intended for any clinical use.
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