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MYO7A Knockout Cell Lines

Gene: MYO7A

Official Full Name: myosin VIIAprovided by HGNC

Gene Summary: This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO01750 MYO7A Knockout cell line (HCT 116) Human MYO7A 1:2~1:4 Negative Online Inquiry
KO01751 MYO7A Knockout cell line (HEK293) Human MYO7A 1:3~1:6 Negative Online Inquiry
KO01752 MYO7A Knockout cell line (A549) Human MYO7A 1:3~1:4 Negative Online Inquiry

Background

MYO7A Gene Knockout Cell Lines are specifically engineered cellular models designed to facilitate the study of the MYO7A gene, which encodes for myosin VIIA, an essential protein involved in cellular transport processes and sensory cell function. Utilizing CRISPR/Cas9 gene-editing technology, these cell lines have been crafted to harbor precise deletions in the MYO7A gene, resulting in knockout models that eliminate gene expression. This allows researchers to investigate the functional pathways associated with myosin VIIA, particularly in the context of auditory and vestibular systems, where mutations in this gene are known to contribute to various inherited forms of hearing loss.

The primary function of MYO7A Gene Knockout Cell Lines is to serve as a robust platform for understanding the pathophysiology underlying MYO7A-related disorders. By characterizing these cell lines, researchers can delve into cellular mechanisms such as intracellular transport, cell adhesion, and sensory signal transduction, which are crucial for auditory function. The distinct absence of myosin VIIA provides a clear experimental framework to elucidate compensatory mechanisms and the impact of gene disruption on cellular behavior.

Scientifically, these knockout cell lines are significant for their applications in both research and clinical settings. They enable the exploration of gene therapy approaches, drug screening, and the development of therapeutic interventions for conditions linked to MYO7A mutations. Moreover, they play an invaluable role in advancing our understanding of molecular pathways implicated in cell motility and growth, which can contribute to broader fields such as cancer research and neurobiology.

Compared to alternative models such as wild-type cell lines or transgenic models, MYO7A Gene Knockout Cell Lines offer an unparalleled specificity for studying the consequences of MYO7A loss. These lines exhibit reproducible and consistent phenotypic outcomes, which enhances experimental reliability and provides a clear basis for comparative analysis.

For researchers and clinicians focused on sensory disorders, genetic disorders, or cellular transport phenomena, MYO7A Gene Knockout Cell Lines represent a crucial resource that simplifies the examination of complex biological interactions. By integrating these models into their studies, users can accelerate their discoveries and contribute meaningfully to the field of genetics and beyond.

Our company leverages years of expertise in genetic engineering and cell line development to provide high-quality biological products that empower the scientific community. We are committed to supporting researchers with innovative tools that facilitate breakthroughs in understanding human health and disease.

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

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