Gene: MYL6
Official Full Name: myosin light chain 6provided by HGNC
Gene Summary: Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain that is expressed in smooth muscle and non-muscle tissues. Genomic sequences representing several pseudogenes have been described and two transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36515 | MYL6 Knockout cell line (HeLa) | Human | MYL6 | 1:3~1:6 | Negative | Online Inquiry |
KO36516 | MYL6 Knockout cell line (HCT 116) | Human | MYL6 | 1:2~1:4 | Negative | Online Inquiry |
KO36517 | MYL6 Knockout cell line (HEK293) | Human | MYL6 | 1:3~1:6 | Negative | Online Inquiry |
KO36518 | MYL6 Knockout cell line (A549) | Human | MYL6 | 1:3~1:4 | Negative | Online Inquiry |
MYL6 Gene Knockout Cell Lines are precisely engineered cellular models designed to facilitate the study of the MYL6 gene's function, which encodes a muscle-specific regulatory light chain protein involved in the actin-myosin interaction crucial for muscle contraction. These knockout cell lines have been developed using CRISPR-Cas9 technology, enabling the targeted disruption of the MYL6 gene, resulting in a complete loss of expression. This innovative approach offers researchers a powerful tool to elucidate the physiological roles of MYL6, as well as its implications in various myopathies and cardiac disorders.
The primary mechanism of action for the MYL6 gene knockout involves the disruption of transcription and subsequent translation of the MYL6 protein, leading to altered muscle contractility and intracellular signaling pathways. By using these knockout cell lines, researchers can investigate the downstream effects on muscle development, functional assays assessing contractility, and gene expression profiles associated with muscle differentiation.
Scientifically, the MYL6 gene knockout cell lines are of immense importance for both basic research and translational studies. They serve as critical models for understanding the etiology of muscular diseases and for developing potential therapeutic strategies, including gene therapy and small molecule interventions. Compared to traditional models, such as whole animal studies, these cell lines provide a more controlled environment, allowing researchers to dissect molecular mechanisms with greater precision.
One of the significant advantages of our MYL6 gene knockout cell lines is their high reproducibility and ease of use, which facilitates consistent experimental outcomes. Additionally, they are validated for multiple applications, including high-throughput screening, co-culture studies, and systems biology approaches, ensuring versatility in different research contexts.
For researchers and clinicians seeking to advance their understanding of muscle biology or to explore innovative therapeutic avenues, our MYL6 gene knockout cell lines represent a valuable addition to their experimental toolkit. By leveraging our cutting-edge biotechnological expertise and commitment to quality, we aim to provide exceptional products that empower scientific discovery and improve health outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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