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ACTA1 Knockout Cell Lines

Gene: ACTA1

Official Full Name: actin alpha 1, skeletal muscleprovided by HGNC

Gene Summary: The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause a variety of myopathies, including nemaline myopathy, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects with manifestations such as hypotonia. [provided by RefSeq, Sep 2019]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO39125 ACTA1 Knockout cell line (HEK293) Human ACTA1 1:3~1:6 Negative Online Inquiry

Background

ACTA1 Gene Knockout Cell Lines are specifically engineered cellular models that lack the expression of the ACTA1 gene, which encodes the skeletal muscle isoform of actin, a crucial protein for muscle contraction and structure. These cell lines serve as invaluable tools for researchers investigating muscle biology, gene function, and the molecular mechanisms underlying various myopathies. By analyzing these knockout lines, researchers can elucidate the role of ACTA1 in muscle development and function, providing insights into genetic disorders associated with muscle weakness or degeneration.

The primary mechanism by which ACTA1 knockout cell lines operate is through the absence of ACTA1 protein expression, resulting in disrupted cytoskeletal integrity and altered cellular signaling pathways related to muscle cell differentiation and maintenance. Researchers can exploit these models to study the specific phenotypic outcomes of ACTA1 deficiency, evaluate the impact of potential therapeutic interventions, and gain a deeper understanding of muscle-related diseases at the cellular level.

Scientifically, these knockout cell lines hold significant importance in both research and clinical settings. They can be employed to investigate various myopathies caused by mutations or dysregulation of the ACTA1 gene, thereby contributing to the development of targeted therapies. Moreover, they serve as a foundation for high-throughput screening of drug candidates to restore normal muscle function or provide insights into novel gene editing strategies aimed at gene correction.

Compared to traditional wild-type cell lines, ACTA1 knockout models offer a distinct advantage by providing clarity in experimental outcomes related to ACTA1 function, enabling researchers to draw more direct conclusions about gene function in a controlled environment. The specificity of these models allows for more precise experimental designs and results, thus enhancing the reliability of research findings in muscle biology.

The value of ACTA1 Gene Knockout Cell Lines extends beyond basic research; they facilitate the exploration of gene therapies and regenerative medicine approaches that could pave the way for innovative treatments in clinical practice. Researchers and clinicians seeking to understand muscle pathology or develop therapeutic interventions will find these cell lines indispensable.

Our company specializes in providing high-quality biological research tools, ensuring that scientists have access to the most cutting-edge models to enhance their research capabilities and breakthroughs in understanding complex biological systems.

Please note that all services are for research use only. Not intended for any clinical use.

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