Gene: RYR1
Official Full Name: ryanodine receptor 1provided by HGNC
Gene Summary: This gene encodes a ryanodine receptor found in skeletal muscle. The encoded protein functions as a calcium release channel in the sarcoplasmic reticulum but also serves to connect the sarcoplasmic reticulum and transverse tubule. Mutations in this gene are associated with malignant hyperthermia susceptibility, central core disease, and minicore myopathy with external ophthalmoplegia. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO08452 | RYR1 Knockout cell line (HCT 116) | Human | RYR1 | 1:2~1:4 | Negative | Online Inquiry |
KO08453 | RYR1 Knockout cell line (A549) | Human | RYR1 | 1:3~1:4 | Negative | Online Inquiry |
RYR1 Gene Knockout Cell Lines are specialized biological products derived from human or animal cell lines in which the RYR1 gene, encoding the ryanodine receptor 1, has been inactivated through precise genetic engineering techniques. These cell lines serve as invaluable tools for investigating the physiological and pathological roles of the RYR1 protein, which is critically involved in calcium homeostasis and muscle contraction. By facilitating the study of RYR1 functions, these knockout models enable researchers to unravel complex mechanisms underlying various myopathies, including malignant hyperthermia and central core disease.
The primary function of RYR1 Gene Knockout Cell Lines lies in their ability to mimic the pathological states linked to RYR1-related disorders. By eliminating the expression of the RYR1 protein, these cell lines provide a controlled environment to observe the downstream effects of calcium dysregulation. Researchers can employ these lines to assess alterations in signaling pathways, gene expression, and muscle cell differentiation, thus enhancing the understanding of muscle physiology and disease.
The scientific importance of RYR1 Gene Knockout Cell Lines extends to both fundamental research and potential clinical applications. In academic settings, they enable the exploration of muscle-related diseases, while in drug development, they could assist in screening compounds for therapeutic efficacy against RYR1 mutations. These cell lines also hold promise for advancing gene therapy strategies aimed at restoring normal calcium signaling.
Compared to alternative models, such as conventional wild-type cell lines, the RYR1 Gene Knockout Cell Lines offer distinct advantages, particularly in specificity and relevance to disease mechanisms. Researchers benefit from the ability to directly manipulate calcium signaling pathways and study the nuances of muscle pathology without confounding variables introduced by functional RYR1 expression.
In conclusion, RYR1 Gene Knockout Cell Lines represent a powerful resource for researchers and clinicians seeking to deepen their understanding of muscle-related diseases and therapeutic interventions. Our company prides itself on advanced genetic engineering capabilities and a commitment to providing high-quality biological products that support cutting-edge research initiatives and clinical discoveries in the field of muscle biology.
Please note that all services are for research use only. Not intended for any clinical use.
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