Gene: PLXNB3
Official Full Name: plexin B3provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the plexin family. It functions as a receptor for semaphorin 5A, and plays a role in axon guidance, invasive growth and cell migration. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36015 | PLXNB3 Knockout cell line (HeLa) | Human | PLXNB3 | 1:3~1:6 | Negative | Online Inquiry |
KO36016 | PLXNB3 Knockout cell line (HCT 116) | Human | PLXNB3 | 1:2~1:4 | Negative | Online Inquiry |
KO36017 | PLXNB3 Knockout cell line (A549) | Human | PLXNB3 | 1:3~1:4 | Negative | Online Inquiry |
PLXNB3 Gene Knockout Cell Lines are genetically modified cell lines designed to elucidate the biological role of the Plexin-B3 gene, a key regulator of cell signaling pathways involved in cell migration, proliferation, and immune responses. By employing advanced CRISPR-Cas9 gene editing technologies, these knockout cell lines offer a powerful tool for researchers to investigate the functional consequences of PLXNB3 suppression. This provides a unique opportunity to explore its implications in various physiological and pathological processes, including cancer metastasis and developmental biology.
The mechanism through which the PLXNB3 gene influences cellular behavior is intricately tied to its role as a receptor for semaphorins, which are critical for neuronal and immune cell signaling. The knockout cell lines facilitate studies on the downstream effects of this signaling cascade, allowing researchers to dissect how the absence of PLXNB3 alters cell behavior and interactions. The relevance of these findings extends to potential therapeutic strategies, as understanding the gene’s function could inform the development of novel treatments for diseases related to aberrant cell signaling.
One of the primary advantages of using PLXNB3 Gene Knockout Cell Lines lies in their specificity and efficiency. Unlike traditional knockdown approaches, which can lead to incomplete gene silencing, these knockout lines enable precise, stable genetic modifications. This reliability enhances experimental reproducibility and supports more definitive conclusions in research outcomes. Furthermore, their compatibility with a wide range of experimental models and assays makes them versatile tools in both academic and clinical research settings.
For researchers and clinicians aiming to investigate gene function, assess drug responses, or understand disease mechanisms, PLXNB3 Gene Knockout Cell Lines represent an invaluable resource. Their ability to mimic disease states in a controlled environment accelerates discovery and therapeutic innovation. Our company is committed to advancing scientific research by providing high-quality, reliable biological products that empower researchers to unlock new biological insights. With our expertise in genetic engineering and a focus on delivering exceptional value, we are dedicated to supporting the scientific community in its quest for knowledge.
Please note that all services are for research use only. Not intended for any clinical use.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
There is no product in your cart. |
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.