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OCRL Knockout Cell Lines

Gene: OCRL

Official Full Name: OCRL inositol polyphosphate-5-phosphataseprovided by HGNC

Gene Summary: This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and, endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO07919 OCRL Knockout cell line (HeLa) Human OCRL 1:3~1:6 Negative Online Inquiry
KO07920 OCRL Knockout cell line (HCT 116) Human OCRL 1:2~1:4 Negative Online Inquiry
KO07921 OCRL Knockout cell line (HEK293) Human OCRL 1:3~1:6 Negative Online Inquiry
KO07922 OCRL Knockout cell line (A549) Human OCRL 1:3~1:4 Negative Online Inquiry

Background

OCRL Gene Knockout Cell Lines are specially engineered cellular models designed to facilitate research in the fields of gene function, cellular signaling, and disease pathology by precisely inactivating the OCRL gene. The OCRL gene encodes an inositol phosphate 5-phosphatase that is implicated in various cellular processes, including endocytosis, cytoskeletal organization, and cell signaling. By utilizing state-of-the-art CRISPR/Cas9 gene-editing technology, these cell lines provide researchers with a robust platform to study the functional consequences of OCRL loss in a controlled laboratory setting.

The primary mechanism of the OCRL Gene Knockout Cell Lines involves targeted genomic alteration, where the OCRL gene is disrupted, leading to observable changes in cellular function and phenotypic expression. This allows scientists to investigate the biological pathways that are affected when OCRL activity is absent, shedding light on its role in diseases such as Dent's disease and other genetic disorders. Researchers can utilize these cell lines to conduct high-throughput screening, drug response studies, and the evaluation of compensatory mechanisms during OCRL loss, significantly advancing our understanding of associated molecular pathways.

The scientific importance of OCRL Gene Knockout Cell Lines extends to both basic and applied research, providing insights into the mechanisms of pathophysiological conditions and potential therapeutic targets. Compared to traditional methods of gene silencing, such as RNA interference, knockout cell lines offer a permanent alteration in the genome, thus providing a more stable platform for long-term studies and therapeutic development.

For researchers and clinicians alike, the advantages of using OCRL Gene Knockout Cell Lines include the ability to yield reproducible results and a clear model for studying the consequences of gene loss over time. The unique selling points stem from their high specificity, ease of integration into existing workflows, and potential to translate findings into clinical applications for targeted therapies.

By choosing OCRL Gene Knockout Cell Lines, users gain access to cutting-edge tools that are not only scientifically validated but also pivotal in advancing our knowledge of genetic conditions and potential interventional strategies. Our company prides itself on expertise in genetic engineering and commitment to delivering high-quality biological products that empower research communities globally.

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

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