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PLXNB1 Knockout Cell Lines

Gene: PLXNB1

Official Full Name: plexin B1provided by HGNC

Gene Summary: Enables semaphorin receptor activity. Involved in several processes, including negative regulation of cell adhesion; regulation of cell shape; and semaphorin-plexin signaling pathway. Located in plasma membrane. Part of semaphorin receptor complex. [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
KO06665 PLXNB1 Knockout cell line (HeLa) Human PLXNB1 1:3~1:6 Negative Online Inquiry
KO06666 PLXNB1 Knockout cell line (HCT 116) Human PLXNB1 1:2~1:4 Negative Online Inquiry
KO06667 PLXNB1 Knockout cell line (HEK293) Human PLXNB1 1:3~1:6 Negative Online Inquiry
KO06668 PLXNB1 Knockout cell line (A549) Human PLXNB1 1:3~1:4 Negative Online Inquiry

Background

PLXNB1 Gene Knockout Cell Lines are genetically engineered models that lack a functional PLXNB1 gene, which encodes for the plexin-B1 protein. This protein plays a critical role in cell signaling pathways, particularly those involved in regulating cell movement, cytoskeletal dynamics, and neuronal development. By creating knockout variants, researchers can study the gene's function and its implications in various biological processes, particularly in cancer biology and neurodevelopmental disorders.

The primary mechanism of action involves the disruption of the PLXNB1 gene, which leads to the absence of its protein product, allowing for the assessment of changes in cellular behavior, signaling pathways, and phenotypic characteristics. This cell line can be utilized to investigate how the loss of PLXNB1 influences processes such as migration, invasion, and neuronal differentiation, providing valuable insights into the underlying mechanisms of disease and developmental biology.

Scientifically, PLXNB1 Gene Knockout Cell Lines are of significant importance for both fundamental research and potential therapeutic applications. These lines facilitate the exploration of novel therapeutic targets in cancer, where aberrant signaling through the PLXNB1 pathway may contribute to tumorigenesis, as well as in neurobiology, where understanding the role of cell signaling in neuronal development is crucial.

One of the key advantages of using our PLXNB1 Gene Knockout Cell Lines is the high specificity and efficiency achieved through advanced CRISPR/Cas9 gene editing techniques. This precision minimizes off-target effects, allowing researchers to obtain reliable and reproducible results. Furthermore, these cell lines are readily available and extensively characterized, saving researchers time and resources typically associated with developing their own knockout models.

For researchers and clinicians, the value of PLXNB1 Gene Knockout Cell Lines lies in their ability to shed light on the complexities of gene function and cell behavior in a controlled environment. This product not only enhances the understanding of critical biological pathways but also opens avenues for the development of innovative therapeutic strategies. Our company is committed to advancing scientific discovery by providing high-quality, reliable biological products that empower research communities worldwide.

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

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