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DIAPH1 Knockout Cell Lines

Gene: DIAPH1

Official Full Name: diaphanous related formin 1provided by HGNC

Gene Summary: This gene is a homolog of the Drosophila diaphanous gene, and has been linked to autosomal dominant, fully penetrant, nonsyndromic sensorineural progressive low-frequency hearing loss. Actin polymerization involves proteins known to interact with diaphanous protein in Drosophila and mouse. It has therefore been speculated that this gene may have a role in the regulation of actin polymerization in hair cells of the inner ear. Alternatively spliced transcript variants encoding distinct isoforms have been found 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
KO03626 DIAPH1 Knockout cell line (HeLa) Human DIAPH1 1:3~1:6 Negative Online Inquiry
KO03627 DIAPH1 Knockout cell line (HCT 116) Human DIAPH1 1:2~1:4 Negative Online Inquiry
KO03628 DIAPH1 Knockout cell line (HEK293) Human DIAPH1 1:3~1:6 Negative Online Inquiry
KO03629 DIAPH1 Knockout cell line (A549) Human DIAPH1 1:3~1:4 Negative Online Inquiry

Background

DIAPH1 Gene Knockout Cell Lines are genetically engineered cell lines designed to specifically lack the expression of the DIAPH1 gene. This gene plays a critical role in regulating actin dynamics and cellular morphology, making these knockout cell lines invaluable for studying cellular processes such as cellular motility, cytoskeleton organization, and signal transduction pathways. By analyzing these cell lines, researchers can investigate the downstream effects of DIAPH1 loss on various biological functions, offering insights into conditions where dysregulation of cytoskeletal dynamics is implicated.

The mechanisms underlying the functionality of these knockout cell lines involve targeted gene editing using techniques such as CRISPR/Cas9, which allows for precise disruption of the DIAPH1 gene with high specificity. This technology enables researchers to create isogenic models wherein the only variable is the presence or absence of DIAPH1, thus facilitating robust experimental designs that can accurately attribute observed phenotypic changes directly to the genetic modification.

From a scientific standpoint, DIAPH1 Gene Knockout Cell Lines hold significant potential in both basic research and clinical applications. They are crucial for investigating diseases characterized by cytoskeletal abnormalities, such as certain cancer types and genetic disorders. Additionally, these cell lines can serve as a platform for drug discovery, enabling high-throughput screening for compounds that target cytoskeletal dynamics.

What sets DIAPH1 Gene Knockout Cell Lines apart from alternative models is their specificity and ease of use. Unlike general cytoskeletal inhibitors, which may elicit off-target effects, these cell lines provide a controlled environment for in-depth analysis of DIAPH1-related pathways, enhancing the reproducibility and applicability of research findings.

For researchers and clinicians, the value of DIAPH1 Gene Knockout Cell Lines lies in their ability to unlock new avenues of exploration in cell biology, provide clarity on disease mechanisms, and contribute to the development of novel therapeutic strategies. Our company, with its expertise in genome editing technologies and a commitment to producing high-quality biological products, is proud to offer these advanced cell lines, empowering the scientific community to push the boundaries of knowledge in the field of cellular biology.

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

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