Gene: PHEX
Official Full Name: phosphate regulating endopeptidase X-linkedprovided by HGNC
Gene Summary: The protein encoded by this gene is a transmembrane endopeptidase that belongs to the type II integral membrane zinc-dependent endopeptidase family. The protein is thought to be involved in bone and dentin mineralization and renal phosphate reabsorption. Mutations in this gene cause X-linked hypophosphatemic rickets. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO04382 | PHEX Knockout cell line (HeLa) | Human | PHEX | 1:3~1:6 | Negative | Online Inquiry |
PHEX Gene Knockout Cell Lines are specially developed cellular models in which the PHEX gene has been functionally disrupted. This gene plays a crucial role in the regulation of phosphate metabolism and its deficiency is associated with conditions such as X-linked hypophosphatemia (XLH). By providing these knockout cell lines, researchers can effectively study the biological processes influenced by PHEX, including bone mineralization and cellular signaling pathways involved in phosphate homeostasis.
The key function of PHEX Gene Knockout Cell Lines lies in their ability to mimic the pathological conditions observed in XLH, offering a controlled environment to elucidate the mechanisms underlying this disorder. Through the loss of PHEX expression, scientists can evaluate the resultant biochemical changes, cellular behaviors, and therapeutic responses, facilitating drug development and gene therapy strategies.
The scientific importance of these cell lines extends to both basic research and translational applications. They serve as an invaluable tool in exploring potential therapeutic interventions, particularly in understanding how interventions can restore phosphate balance in affected individuals. Moreover, these cell lines can be used to assess the efficacy of novel compounds in clinical trials, thereby bridging the gap between laboratory findings and patient treatments.
Compared to traditional cell models, PHEX Gene Knockout Cell Lines offer a greater specificity and relevance to human disease mechanisms, making them superior for researchers investigating phosphate metabolism. Additionally, their reliable reproducibility and defined genetic modifications provide researchers with consistent and high-quality data.
Utilizing PHEX Gene Knockout Cell Lines adds significant value to any research endeavor focused on phosphate regulation disorders. They empower researchers and clinicians to unlock new insights into the underlying pathophysiology of these conditions, potentially leading to innovative therapeutic strategies.
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Please note that all services are for research use only. Not intended for any clinical use.
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