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PLEKHB2 Knockout Cell Lines

Gene: PLEKHB2

Official Full Name: pleckstrin homology domain containing B2provided by HGNC

Gene Summary: Enables phosphatidylinositol-3,4,5-trisphosphate binding activity. Predicted to be involved in regulation of cell differentiation. Predicted to be located in recycling endosome membrane. Predicted to be active in membrane. [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
KO15070 PLEKHB2 Knockout cell line (HeLa) Human PLEKHB2 1:3~1:6 Negative Online Inquiry
KO15071 PLEKHB2 Knockout cell line (HCT 116) Human PLEKHB2 1:2~1:4 Negative Online Inquiry
KO15072 PLEKHB2 Knockout cell line (HEK293) Human PLEKHB2 1:3~1:6 Negative Online Inquiry
KO15073 PLEKHB2 Knockout cell line (A549) Human PLEKHB2 1:3~1:4 Negative Online Inquiry

Background

PLEKHB2 Gene Knockout Cell Lines are innovative biological tools derived from specific cell types that have undergone targeted gene disruption, specifically at the PLEKHB2 locus. PLEKHB2, a gene known to be involved in a variety of cellular processes including cytoskeletal organization and intracellular signaling, is crucial for understanding the molecular mechanisms underlying several physiological and pathological states. These knockout cell lines enable researchers to dissect the role of PLEKHB2 in various cellular functions, providing a robust platform for functional genomics studies.

The primary function of these cell lines is to facilitate the exploration of gene function through loss-of-function studies. By knocking out the PLEKHB2 gene, researchers can investigate changes in cellular behavior, such as alterations in migration, adhesion, and response to environmental stimuli. The specific mechanisms involve employing CRISPR/Cas9 technology or similar gene-editing techniques to create precise modifications, ensuring that the cellular responses observed are directly attributed to the absence of PLEKHB2.

The scientific importance of PLEKHB2 Gene Knockout Cell Lines lies in their potential applications in both basic and translational research settings. They can significantly aid in elucidating the role of PLEKHB2 in diseases such as cancer, neurodegenerative disorders, and metabolic dysregulation, establishing a clear link between gene function and pathology. Additionally, their use in drug discovery and development processes allows for the identification of novel therapeutic targets related to PLEKHB2-associated pathways.

Compared to alternative models like wild-type cell lines or knock-in models, these knockout lines offer a clear advantage by providing a direct assessment of the PLEKHB2 gene's role without the confounding effects that may arise from the presence of functional alleles. Their specificity allows for more accurate and reproducible results, vital in elucidating gene-function relationships.

Researchers, clinicians, and biopharmaceutical companies stand to gain substantial insights from the use of PLEKHB2 Gene Knockout Cell Lines, as they enhance the understanding of gene function in disease and facilitate the development of targeted therapeutics. This product, backed by our company’s strong track record in genetic engineering and cell line development, is an invaluable resource for any research aiming for depth and clarity in gene-function analysis. Our expertise ensures that these knockout cell lines are of the highest quality and ready to meet rigorous scientific standards.

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

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