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JAM3 Knockout Cell Lines

Gene: JAM3

Official Full Name: junctional adhesion molecule 3provided by HGNC

Gene Summary: Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. The protein encoded by this immunoglobulin superfamily gene member is localized in the tight junctions between high endothelial cells. Unlike other proteins in this family, the this protein is unable to adhere to leukocyte cell lines and only forms weak homotypic interactions. The encoded protein is a member of the junctional adhesion molecule protein family and acts as a receptor for another member of this family. A mutation in an intron of this gene is associated with hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Apr 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO01052 JAM3 Knockout cell line (HCMEC/D3) Human JAM3 1:3~1:4 Negative Online Inquiry
KO01264 JAM3 Knockout cell line (MDCK) Dog JAM3 Negative Online Inquiry
KO25395 JAM3 Knockout cell line (HEK293) Human JAM3 1:3~1:6 Negative Online Inquiry
KO25396 JAM3 Knockout cell line (A549) Human JAM3 1:3~1:4 Negative Online Inquiry

Background

JAM3 Gene Knockout Cell Lines are a powerful tool in molecular biology, designed to facilitate the study of the Junctional Adhesion Molecule 3 (JAM3), a protein implicated in various physiological and pathological processes, including immune response and tumor progression. These cell lines are genetically modified to lack the expression of the JAM3 gene, allowing researchers to dissect the protein's role in cell adhesion, migration, and signaling pathways with unprecedented clarity.

The key functionality of JAM3 Gene Knockout Cell Lines lies in their ability to provide a controlled environment to observe the phenotypic and physiological consequences of the absence of JAM3. By utilizing CRISPR-Cas9 gene editing technology, these cell lines enable precise and efficient targeting of the JAM3 gene, ensuring that researchers can confidently assess the downstream effects on cellular behavior. The absence of JAM3 allows for the evaluation of alterations in cell-cell interactions, immune cell trafficking, and the overall impact of JAM3 in various models of disease.

Scientifically, the importance of studying JAM3 cannot be understated, as its dysregulation has been implicated in inflammatory diseases and cancer. These knockout cell lines have vast applications in both basic research, elucidating cellular mechanisms, and clinical settings, where they support the development of therapeutic interventions targeting JAM3-related pathways. Furthermore, they serve as indispensable resources for drug screening and testing the efficacy of novel therapeutic agents.

The unique selling points of JAM3 Gene Knockout Cell Lines include their reliable genetic modification and the robustness of the experimental outcomes they provide. Unlike other alternatives that may rely on transient knockdown methods, these knockout cell lines guarantee stable gene disruption, allowing for more reproducible and consistent results. This stability is crucial for long-term studies and real-time monitoring of cellular changes over extended periods.

For researchers and clinicians focused on advancing their understanding of JAM3's role in health and disease, JAM3 Gene Knockout Cell Lines offer an unparalleled opportunity to investigate complex biological questions with clarity and precision. Our company boasts a strong foundation in genetic engineering and cellular biology, ensuring that these cell lines are created with the highest quality standards in mind, thereby empowering researchers to achieve their scientific objectives effectively.

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

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