Gene: TNNC1
Official Full Name: troponin C1, slow skeletal and cardiac typeprovided by HGNC
Gene Summary: Troponin is a central regulatory protein of striated muscle contraction, and together with tropomyosin, is located on the actin filament. Troponin consists of 3 subunits: TnI, which is the inhibitor of actomyosin ATPase; TnT, which contains the binding site for tropomyosin; and TnC, the protein encoded by this gene. The binding of calcium to TnC abolishes the inhibitory action of TnI, thus allowing the interaction of actin with myosin, the hydrolysis of ATP, and the generation of tension. Mutations in this gene are associated with cardiomyopathy dilated type 1Z. [provided by RefSeq, Oct 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO07986 | TNNC1 Knockout cell line (HeLa) | Human | TNNC1 | 1:3~1:6 | Negative | Online Inquiry |
KO07987 | TNNC1 Knockout cell line (HCT 116) | Human | TNNC1 | 1:2~1:4 | Negative | Online Inquiry |
KO07988 | TNNC1 Knockout cell line (HEK293) | Human | TNNC1 | 1:3~1:6 | Negative | Online Inquiry |
KO07989 | TNNC1 Knockout cell line (A549) | Human | TNNC1 | 1:3~1:4 | Negative | Online Inquiry |
TNNC1 Gene Knockout Cell Lines represent a groundbreaking tool in the field of molecular biology, specifically designed to facilitate the study of troponin C (TNNC1) and its role in cardiac physiology and pathology. These cell lines have been genetically engineered to permanently disrupt the TNNC1 gene, thereby eliminating the expression of its protein product. This knockout approach enables researchers to investigate the downstream effects of TNNC1 deficiency on cardiac muscle contraction and calcium signaling, assisting in elucidating the molecular mechanisms underlying various cardiovascular diseases.
The key function of these cell lines lies in their ability to provide a controlled environment for the examination of cardiac myocyte functions in the absence of TNNC1. By utilizing techniques such as CRISPR-Cas9 for precise genome editing, the knockout cells exhibit marked alterations in contractile properties and response to calcium ions, serving as essential models for studying hypertrophic cardiomyopathy and other related conditions. This targeted manipulation of gene expression allows for a refined analysis of signaling pathways that contribute to heart diseases, which is crucial for developing potential therapeutic interventions.
In research settings, TNNC1 Gene Knockout Cell Lines are invaluable for drug discovery and testing, offering a platform to screen compounds that may correct or compensate for the dysfunction caused by TNNC1 loss. Additionally, they serve as a pivotal resource for academic institutions and industrial labs focused on cardiovascular research, aiming to bridge translational science with clinical applications.
What sets these knockout cell lines apart from traditional models is their specificity and reliability. Unlike whole organism studies or heterogeneous cell populations, TNNC1 knockout cell lines provide a consistent, homogenous system for experimentation. Furthermore, the ease of use in various assays—including electrophysiology and calcium imaging—enhances their appeal, making them user-friendly even for laboratories with limited experience in genetic engineering.
For researchers and clinicians, the TNNC1 Gene Knockout Cell Lines are not just a product; they represent a strategic investment in advanced research capabilities that can lead to significant breakthroughs in understanding heart disease mechanisms. With a commitment to innovation and quality, our company specializes in providing cutting-edge biological tools designed to accelerate scientific inquiry and improve therapeutic outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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