Gene: SCN9A
Official Full Name: sodium voltage-gated channel alpha subunit 9provided by HGNC
Gene Summary: This gene encodes a voltage-gated sodium channel which plays a significant role in nociception signaling. Mutations in this gene have been associated with primary erythermalgia, channelopathy-associated insensitivity to pain, and paroxysmal extreme pain disorder. [provided by RefSeq, Aug 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO01640 | SCN9A Knockout cell line (HeLa) | Human | SCN9A | 1:3~1:6 | Negative | Online Inquiry |
KO01641 | SCN9A Knockout cell line (HEK293) | Human | SCN9A | 1:3~1:6 | Negative | Online Inquiry |
KO01642 | SCN9A Knockout cell line (A549) | Human | SCN9A | 1:3~1:4 | Negative | Online Inquiry |
SCN9A Gene Knockout Cell Lines are specially engineered human or animal cell lines in which the SCN9A gene, encoding the voltage-gated sodium channel NaV1.7, has been functionally disrupted. This genetic modification enables a controlled environment to study the physiological and pathological roles of NaV1.7, which has been implicated in pain signaling and sensory neuron function. These knockout cell lines serve as a crucial tool for dissecting the molecular mechanisms underlying nociception, leading to a deeper understanding of pain pathways and potential therapeutic targets.
The primary function of SCN9A Gene Knockout Cell Lines is to facilitate the examination of NaV1.7's contributions to pain perception. By observing the functional output of cells lacking this channel, researchers can investigate pain-induced cellular responses, neurotransmitter release, and action potential firing patterns without the confounding influences of NaV1.7 activity. This precise modeling enhances the ability to identify novel analgesic compounds or conduct gene therapy studies with a clearer focus on pain mechanisms.
The scientific importance of these cell lines extends to both basic research and clinical applications. In research settings, they are indispensable for elucidating the genetic and molecular pathways associated with inherited pain disorders, such as primary erythermalgia and inherited neuropathy. Clinically, insights gained from these studies could lead to the development of targeted pain management strategies, improving the quality of life for patients suffering from chronic pain conditions.
Compared to conventional methods that rely on wild-type cells, SCN9A Gene Knockout Cell Lines offer unrivaled specificity in studying the direct effects of NaV1.7 absence. This specificity not only enables researchers to pinpoint the channel’s contribution to pain but also minimizes off-target effects often encountered with pharmacological agents. Furthermore, the use of these knockout lines can significantly streamline the drug discovery process by enhancing assay accuracy and reproducibility.
For researchers, clinicians, and pharmaceutical companies, SCN9A Gene Knockout Cell Lines provide a rich platform for innovative investigation into pain mechanisms and drug development. Their application could yield breakthroughs in pain management and treatment modalities, underscoring their value in advancing scientific understanding and patient care.
Our company has a long-standing commitment to providing high-quality biological research products and cutting-edge genetic engineering solutions that empower the scientific community. With extensive expertise in gene editing technologies, we ensure that your research efforts are equipped with reliable and effective tools, driving forward the frontiers of medical science.
Please note that all services are for research use only. Not intended for any clinical use.
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