Gene: PMP22
Official Full Name: peripheral myelin protein 22provided by HGNC
Gene Summary: This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35995 | PMP22 Knockout cell line (HeLa) | Human | PMP22 | 1:3~1:6 | Negative | Online Inquiry |
KO35996 | PMP22 Knockout cell line (HCT 116) | Human | PMP22 | 1:2~1:4 | Negative | Online Inquiry |
KO35997 | PMP22 Knockout cell line (HEK293) | Human | PMP22 | 1:3~1:6 | Negative | Online Inquiry |
KO35998 | PMP22 Knockout cell line (A549) | Human | PMP22 | 1:3~1:4 | Negative | Online Inquiry |
PMP22 gene knockout cell lines are genetically engineered cellular models specifically designed to study the role and function of the PMP22 gene, which encodes for a vital protein involved in myelin sheath formation around peripheral nerves. These knockout cell lines feature targeted deletions of the PMP22 gene, allowing researchers to observe the resultant phenotypic and molecular changes, particularly in the context of neuropathies such as Charcot-Marie-Tooth disease. By specifically eliminating the expression of PMP22, these cell lines serve as an invaluable tool for elucidating the gene's contribution to cellular homeostasis, signaling pathways, and myelination processes.
The mechanism behind the function of PMP22 gene knockout cell lines lies in their ability to mimic pathological conditions in vitro, thereby offering insights into the mechanisms driving demyelinating diseases. Researchers can utilize these cell lines to conduct functional assays, protein expression studies, and drug screening for potential therapeutic interventions. In clinical settings, these models can play a crucial role in preclinical research by providing evidence and support for emerging treatments aimed at correcting or compensating for PMP22-related dysfunctions.
Compared to other models, the PMP22 gene knockout cell lines provide a more specific and relevant platform for studying peripheral nerve diseases, as their genetic modification directly targets the gene of interest. This specificity enhances the reproducibility and relevance of experimental outcomes, giving researchers confidence in their findings. Furthermore, unlike broader models that may introduce confounding variables, these cell lines offer a controlled environment conducive to focused investigations.
The value of PMP22 gene knockout cell lines extends beyond basic research; they are essential for developing novel strategies for diagnosing and treating neuropathies linked to PMP22 dysfunction and for advancing our understanding of peripheral nerve biology. Researchers and clinicians can leverage these models to facilitate the discovery of biomarkers and therapeutic targets, fostering innovative solutions to pressing health challenges.
With our company’s commitment to advancing biological research through high-quality products, we provide unparalleled expertise and support for the utilization of PMP22 gene knockout cell lines, ensuring that researchers are equipped with the best tools for success in their studies.
Please note that all services are for research use only. Not intended for any clinical use.
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