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FANCB Knockout Cell Lines

Gene: FANCB

Official Full Name: FA complementation group Bprovided by HGNC

Gene Summary: This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO37912 FANCB Knockout cell line (HeLa) Human FANCB 1:3~1:6 Negative Online Inquiry
KO37913 FANCB Knockout cell line (HCT 116) Human FANCB 1:2~1:4 Negative Online Inquiry
KO37914 FANCB Knockout cell line (HEK293) Human FANCB 1:3~1:6 Negative Online Inquiry
KO37915 FANCB Knockout cell line (A549) Human FANCB 1:3~1:4 Negative Online Inquiry

Background

FANCB Gene Knockout Cell Lines are specialized cell lines that have undergone targeted genetic modification to disrupt the function of the FANCB gene, an essential component of the Fanconi anemia (FA) pathway. This gene plays a critical role in DNA repair mechanisms, particularly in response to interstrand crosslinks and various DNA-damaging agents. These knockout cell lines serve as powerful tools for studying the biological functions of FANCB, elucidating the molecular basis of Fanconi anemia, and investigating cellular responses to DNA damage.

The mechanism by which FANCB gene knockout cell lines operate revolves around the loss of the FANCB protein, leading to impaired DNA repair processes. This deficiency results in heightened sensitivity to agents that induce DNA crosslinking, thus enabling researchers to assess the functional consequences of FANCB loss. The cell lines also provide a platform for exploring the interplay between DNA repair and other cellular pathways, contributing to the understanding of genetic stability in both normal and cancerous cells.

The scientific significance of FANCB Gene Knockout Cell Lines lies in their broad application in biomedical research and therapeutic development. They are invaluable for drug screening, gene therapy investigations, and preclinical studies aimed at developing targeted treatments for Fanconi anemia and related malignancies. These cell lines facilitate the exploration of small molecules and other experimental therapies designed to enhance DNA repair capabilities or sensitize cells to chemotherapy.

What sets FANCB Gene Knockout Cell Lines apart from alternatives is their precision in editing the FANCB gene without off-target effects, ensuring reliable and reproducible results. Furthermore, researchers gain insights into crucial cellular mechanisms previously obscured by the presence of endogenous FANCB, allowing for clearer interpretation of experimental outcomes.

For researchers and clinicians looking to deepen their understanding of DNA repair mechanisms and develop potential therapeutic strategies, FANCB Gene Knockout Cell Lines offer unparalleled value. They empower investigations into the pathophysiology of Fanconi anemia and associated cancers, fostering innovation in clinical applications.

Our company stands at the forefront of genetic engineering and cell line development, leveraging cutting-edge technology and extensive expertise to provide high-quality biological products. With FANCB Gene Knockout Cell Lines, we are committed to supporting your research endeavors with the tools needed to advance scientific discovery and therapeutic innovation.

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

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