Gene: RNF213
Official Full Name: ring finger protein 213provided by HGNC
Gene Summary: This gene encodes a protein containing a C3HC4-type RING finger domain, which is a specialized type of Zn-finger that binds two atoms of zinc and is thought to be involved in mediating protein-protein interactions. The protein also contains an AAA domain, which is associated with ATPase activity. This gene is a susceptibility gene for Moyamoya disease, a vascular disorder of intracranial arteries. This gene is also a translocation partner in anaplastic large cell lymphoma and inflammatory myofibroblastic tumor cases, where a t(2;17)(p23;q25) translocation has been identified with the anaplastic lymphoma kinase (ALK) gene on chromosome 2, and a t(8;17)(q24;q25) translocation has been identified with the MYC gene on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO06856 | RNF213 Knockout cell line (HeLa) | Human | RNF213 | 1:3~1:6 | Negative | Online Inquiry |
KO06857 | RNF213 Knockout cell line (HCT 116) | Human | RNF213 | 1:2~1:4 | Negative | Online Inquiry |
KO06858 | RNF213 Knockout cell line (HEK293) | Human | RNF213 | 1:3~1:6 | Negative | Online Inquiry |
KO06859 | RNF213 Knockout cell line (A549) | Human | RNF213 | 1:3~1:4 | Negative | Online Inquiry |
RNF213 Gene Knockout Cell Lines are specialized cellular models engineered to lack the RNF213 gene, which has been associated with susceptibility to various vascular and neurovascular disorders, including moyamoya disease. These cell lines serve as an invaluable tool for researchers seeking to dissect the roles of RNF213 in cellular and molecular pathways. The gene encodes an E3 ubiquitin ligase that plays a crucial role in protein degradation and cellular stress responses, making its knockout instrumental in elucidating the pathophysiological mechanisms underlying its associated conditions.
The primary function of the RNF213 knockout cell lines is to provide insights into the biological processes impacted by the absence of this gene. By studying these cell lines, researchers can explore altered signaling pathways, gene expression profiles, and cellular responses to various stimuli, thereby enhancing their understanding of vascular integrity and neurodegenerative mechanisms.
Scientifically, the applications of RNF213 gene knockout cell lines span fundamental research to translational studies. They are instrumental in developing targeted therapies and novel diagnostic tools, ultimately leading to improved patient outcomes. In clinical settings, understanding the functional consequences of RNF213 knockout can pave the way for personalized medicine approaches in treating vascular disorders.
What sets our RNF213 Gene Knockout Cell Lines apart from alternatives is the rigor in their validation and the high specificity of the knockout, ensuring that researchers achieve reproducible and reliable results. These cell lines are crucial for advancing research while reducing the uncertainty that may arise from using less optimized models.
For researchers and clinicians alike, the RNF213 Gene Knockout Cell Lines provide a robust platform for groundbreaking discoveries. Our company, with years of expertise in genetic engineering and cell line development, remains committed to delivering high-quality biological products that empower the scientific community to advance health science effectively.
Please note that all services are for research use only. Not intended for any clinical use.
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