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MECP2 Knockout Cell Lines

Gene: Mecp2

Official Full Name: methyl CpG binding protein 2provided by MGI

Gene Summary: Enables several functions, including histone reader activity; nucleic acid binding activity; and promoter-specific chromatin binding activity. Involved in several processes, including associative learning; negative regulation of smooth muscle cell differentiation; and negative regulation of transcription by RNA polymerase II. Acts upstream of or within several processes, including learning or memory; nervous system development; and regulation of gene expression. Located in cytosol; heterochromatin; and nucleus. Is expressed in several structures, including alimentary system; early conceptus; nervous system; paraxial mesenchyme; and sensory organ. Used to study Rett syndrome. Human ortholog(s) of this gene implicated in Rett syndrome; autistic disorder; gastrointestinal system disease; severe congenital encephalopathy due to MECP2 mutation; and syndromic X-linked intellectual disability (multiple). Orthologous to human MECP2 (methyl-CpG binding protein 2). [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03110 MECP2 Knockout cell line (HeLa) Human MECP2 1:3~1:6 Negative Online Inquiry
KO03111 MECP2 Knockout cell line (HCT 116) Human MECP2 1:2~1:4 Negative Online Inquiry
KO03112 MECP2 Knockout cell line (HEK293) Human MECP2 1:3~1:6 Negative Online Inquiry
KO03113 MECP2 Knockout cell line (A549) Human MECP2 1:3~1:4 Negative Online Inquiry

Background

Mecp2 Gene Knockout Cell Lines are specifically engineered cellular models that have had the methyl CpG binding protein 2 (MeCP2) gene disrupted through targeted genetic modification techniques, such as CRISPR/Cas9 or homologous recombination. This gene plays a crucial role in neuronal development and function, making these knockout cell lines essential tools for studying various neurological disorders, particularly Rett syndrome, which predominantly affects females and manifests through cognitive and physical impairments.

The primary function of Mecp2 Gene Knockout Cell Lines lies in elucidating the molecular pathways influenced by MeCP2. By being devoid of the functional gene, these cell lines facilitate insights into the regulatory networks that govern gene expression in the central nervous system. The absence of MeCP2 allows researchers to closely examine downstream effects on synaptic function, neural plasticity, and overall cell signaling mechanisms, providing a deeper understanding of the etiology of MeCP2-related disorders.

In both research and clinical applications, these cell lines are invaluable for drug discovery, functional genomics, and gene therapy studies. They enable the assessment of therapeutic candidates, the evaluation of gene editing strategies, and the translation of laboratory findings into potential treatments. Furthermore, Mecp2 Gene Knockout Cell Lines can be utilized in high-throughput screening assays, accelerating the identification of compounds that may restore normal function in affected pathways.

One of the key advantages of using Mecp2 Gene Knockout Cell Lines is the specificity and controlled environment they offer relative to alternative approaches like animal models, which can be cost-prohibitive and ethically complex. By working with cell lines, researchers can obtain reproducible results in a scalable manner, facilitating easier and more efficient experimentation.

The unique selling proposition of these cell lines lies in their ability to provide targeted insights into the multifaceted roles of MeCP2 in neurobiology, ultimately aiding in bridging the gap between basic science and clinical application. These attributes make Mecp2 Gene Knockout Cell Lines an indispensable asset for researchers and clinicians alike, driving impactful advancements in the understanding and treatment of MeCP2-related disorders.

With years of expertise in genetic engineering and a robust portfolio of biologically relevant products, our company is dedicated to providing high-quality and scientifically validated tools that support the innovative research being undertaken in the field of neurobiology and beyond.

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

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