Gene: TPM2
Official Full Name: tropomyosin 2provided by HGNC
Gene Summary: This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO13096 | TPM2 Knockout cell line (HeLa) | Human | TPM2 | 1:3~1:6 | Negative | Online Inquiry |
KO13097 | TPM2 Knockout cell line (HCT 116) | Human | TPM2 | 1:2~1:4 | Negative | Online Inquiry |
KO13098 | TPM2 Knockout cell line (HEK293) | Human | TPM2 | 1:3~1:6 | Negative | Online Inquiry |
KO13099 | TPM2 Knockout cell line (A549) | Human | TPM2 | 1:3~1:4 | Negative | Online Inquiry |
TPM2 Gene Knockout Cell Lines are genetically engineered cell models designed to lack the expression of the TPM2 gene, which encodes the tropomyosin 2 protein. This modification provides researchers with a powerful tool to study the biological functions and pathways regulated by TPM2, particularly its role in muscle contraction, cytoskeletal organization, and cellular motility. By eliminating TPM2 expression, these knockout cell lines serve as an effective system for examining the consequences of loss-of-function mutations, potentially unveiling novel insights into various disease states, including cardiomyopathies and certain forms of cancer.
The key function of these cell lines revolves around the ability to dissect the role of TPM2 in cellular processes. With the absence of tropomyosin 2, researchers can investigate changes in actin filament dynamics, contractility, and cellular signaling pathways that are otherwise masked in wild-type cells. This enables the elucidation of the molecular mechanisms behind muscle disorders and serves as an essential tool for drug discovery and development, allowing for high-throughput screening of therapeutic candidates that target related pathways.
In the realm of scientific importance, TPM2 Gene Knockout Cell Lines are invaluable in both research and clinical settings. They provide a model to study gene function and regulation, contributing to our understanding of genetic mutations and their impact on health. Furthermore, these cell lines can be instrumental in developing therapies that target similar pathways implicated in diverse disorders.
What sets TPM2 Gene Knockout Cell Lines apart from alternative models is the precision of gene editing technology employed, allowing for a complete and specific genetic disruption that enhances reproducibility and reliability in experimental results. This specificity helps to avoid off-target effects often seen in other genetic modification approaches, providing researchers with robust data.
For researchers and clinicians, the value of TPM2 Gene Knockout Cell Lines lies not only in their ability to advance scientific understanding but also in their potential to lead to breakthrough therapeutic strategies. By facilitating the exploration of gene function in health and disease, these cell lines represent an essential component of modern biological research.
Our company is committed to providing high-quality biological tools that empower scientific discovery. With expertise in gene editing technologies and a broad portfolio of products, we enable researchers to achieve new milestones in their work, ensuring they have the best resources available for their critical investigations.
Please note that all services are for research use only. Not intended for any clinical use.
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