Gene: VPS35
Official Full Name: VPS35 retromer complex componentprovided by HGNC
Gene Summary: This gene belongs to a group of vacuolar protein sorting (VPS) genes. The encoded protein is a component of a large multimeric complex, termed the retromer complex, involved in retrograde transport of proteins from endosomes to the trans-Golgi network. The close structural similarity between the yeast and human proteins that make up this complex suggests a similarity in function. Expression studies in yeast and mammalian cells indicate that this protein interacts directly with VPS35, which serves as the core of the retromer complex. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00395 | VPS35 knockout cell line (HEK293) | Human | VPS35 | 1:3~1:6 | Negative | Online Inquiry |
KO12660 | VPS35 Knockout cell line (HeLa) | Human | VPS35 | 1:3~1:6 | Negative | Online Inquiry |
KO12661 | VPS35 Knockout cell line (HCT 116) | Human | VPS35 | 1:2~1:4 | Negative | Online Inquiry |
KO12662 | VPS35 Knockout cell line (A549) | Human | VPS35 | 1:3~1:4 | Negative | Online Inquiry |
VPS35 Gene Knockout Cell Lines are genetically engineered cell lines designed to study the functional role of the VPS35 gene, an essential component of the retromer complex involved in intracellular trafficking and protein sorting. These knockout cell lines are created via CRISPR-Cas9 technology, leading to the precise disruption of the VPS35 gene, allowing researchers to elucidate its specific biological functions and implications in diseases, particularly neurodegenerative disorders such as Alzheimer’s and Parkinson’s disease.
The primary function of VPS35 is to facilitate the retrieval of cargo proteins from endosomes to the trans-Golgi network, thus playing a critical role in maintaining cellular homeostasis. By utilizing VPS35 knockout cell lines, researchers can examine the resultant phenotypic changes in protein trafficking and characterize the downstream effects on cellular signaling pathways. This functional analysis aids in identifying the role of VPS35 in pathologies, potentially revealing novel therapeutic targets.
The scientific importance of these cell lines lies in their capacity to advance our understanding of protein mislocalization and its relationship to certain diseases, making them invaluable tools in both basic research and clinical settings. Compared to traditional methods of gene silencing, such as siRNA or shRNA techniques, VPS35 knockout cell lines provide a more stable and robust platform for long-term studies, increasing the reliability of experimental outcomes.
Moreover, these cell lines are likely to appeal to researchers and clinicians who are seeking to explore new avenues of neurodegenerative disease research. The ability to analyze the functional impairment caused by the absence of VPS35 can yield insights into disease mechanisms and provide a foundation for the development of targeted therapies.
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