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WIPF1 Knockout Cell Lines

Gene: WIPF1

Official Full Name: WAS/WASL interacting protein family member 1provided by HGNC

Gene Summary: This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO34818 WIPF1 Knockout cell line (HeLa) Human WIPF1 1:3~1:6 Negative Online Inquiry
KO34819 WIPF1 Knockout cell line (HEK293) Human WIPF1 1:3~1:6 Negative Online Inquiry
KO34820 WIPF1 Knockout cell line (A549) Human WIPF1 1:3~1:4 Negative Online Inquiry

Background

WIPF1 Gene Knockout Cell Lines are genetically engineered cellular models designed to specifically disrupt the expression of the WIPF1 gene, which encodes the WASP-interacting protein that plays a pivotal role in actin dynamics and various cellular processes. Through the use of advanced CRISPR-Cas9 technology, these cell lines offer researchers a highly effective tool for studying the functional impact of WIPF1 loss on cellular behavior, signal transduction pathways, and other biological processes relevant to health and disease.

The primary function of WIPF1 is to interact with the WASP protein to facilitate actin polymerization, an essential process for numerous cellular activities including migration, morphogenesis, and immune responses. By utilizing WIPF1 knockout cell lines, researchers can investigate the downstream effects of WIPF1 deficiency, including alterations in cytoskeletal structure, changes in cell motility, and the regulation of immune cell responses. This makes them invaluable in cancer research, neurobiology, and investigations into various autoimmune disorders.

The scientific significance of WIPF1 knockout cell lines extends to their applications in drug discovery, disease modeling, and therapeutic development. Researchers can employ these models to better understand the molecular mechanisms that underlie various pathologies, potentially paving the way for novel therapeutic interventions.

Compared to traditional gene silencing methods such as RNA interference, using knockout cell lines offers distinct advantages including complete loss of function and long-term study of phenotype without concerns regarding transient effects or off-target effects commonly associated with RNAi technologies. This specificity enhances the reliability of experimental outcomes, making WIPF1 knockout cell lines a superior choice for rigorous scientific inquiry.

For researchers and clinicians focused on elucidating gene function and disease mechanisms, the value of WIPF1 knockout cell lines lies not just in their design, but also in their potential to uncover new therapeutic targets and inform clinical strategies. Our company specializes in providing high-quality, validated genetic tools tailored for cutting-edge research, ensuring you receive the reliability and expertise necessary to advance your scientific goals.

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

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