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INF2 Knockout Cell Lines

Gene: INF2

Official Full Name: inverted formin 2provided by HGNC

Gene Summary: This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5.[provided by RefSeq, Aug 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03359 INF2 Knockout cell line (HeLa) Human INF2 1:3~1:6 Negative Online Inquiry
KO03360 INF2 Knockout cell line (HCT 116) Human INF2 1:2~1:4 Negative Online Inquiry
KO03361 INF2 Knockout cell line (HEK293) Human INF2 1:3~1:6 Negative Online Inquiry
KO03362 INF2 Knockout cell line (A549) Human INF2 1:3~1:4 Negative Online Inquiry

Background

INF2 Gene Knockout Cell Lines are a sophisticated biological tool designed to facilitate detailed studies of the INF2 gene, which is integral to various cellular processes, including cytoskeletal dynamics and pathogenesis related to certain diseases. These cell lines have been meticulously engineered to contain targeted deletions of the INF2 gene, allowing researchers to dissect the gene's functional roles in cell biology, disease mechanisms, and therapeutic responses.

The primary function of these knockout cell lines involves the examination of the implications of INF2 loss on cellular processes such as proliferation, migration, and apoptosis. Researchers can utilize these models to delve into the mechanistic pathways influenced by INF2, particularly its role as a regulator of actin dynamics and how its dysregulation can lead to disorders like focal segmental glomerulosclerosis (FSGS) and other related health issues. By comparing the behaviors of INF2-deficient cells with their wild-type counterparts, scientists can gain insights into potential pharmacological targets for therapeutic intervention.

The scientific importance of INF2 Gene Knockout Cell Lines cannot be overstated, particularly in research endeavors aimed at understanding cytoskeletal-related diseases. Their applications extend into both basic research settings, where they foster fundamental discoveries in cell biology, and clinical research, where they facilitate the development of targeted therapies and personalized medicine approaches based on genetic insights.

Compared to other genetic manipulation techniques such as CRISPR/Cas9-optimized cell lines, INF2 Gene Knockout Cell Lines offer a high level of specificity and stability, simplifying experimental setups and ensuring reproducibility of results. Moreover, these cell lines enable the assessment of specific gene functions without the complications of off-target effects commonly associated with broader genetic editing techniques.

For researchers and clinicians alike, the value of INF2 Gene Knockout Cell Lines is evident in their ability to elucidate the complexities of gene function within cellular contexts, ultimately bridging the gap between fundamental research and clinical applications. This highlights the potential for groundbreaking discoveries that could pave the way for innovative therapeutic strategies.

[Your Company Name] stands at the forefront of biological product development, offering extensive expertise in genetic manipulation technologies and a commitment to supporting the scientific community with high-quality, reliable products tailored for advanced research and clinical needs.

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

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