Gene: PEX19
Official Full Name: peroxisomal biogenesis factor 19provided by HGNC
Gene Summary: This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35769 | PEX19 Knockout cell line (HeLa) | Human | PEX19 | 1:3~1:6 | Negative | Online Inquiry |
KO35770 | PEX19 Knockout cell line (HCT 116) | Human | PEX19 | 1:2~1:4 | Negative | Online Inquiry |
KO35771 | PEX19 Knockout cell line (HEK293) | Human | PEX19 | 1:3~1:6 | Negative | Online Inquiry |
KO35772 | PEX19 Knockout cell line (A549) | Human | PEX19 | 1:3~1:4 | Negative | Online Inquiry |
PEX19 Gene Knockout Cell Lines are specialized cell line models engineered to study the function and role of the PEX19 gene, which is crucial for peroxisome biogenesis and the import of peroxisomal matrix proteins. These knockout cell lines are created through advanced CRISPR/Cas9 gene-editing technology, effectively removing the PEX19 gene to facilitate the examination of its molecular mechanisms and associated pathways.
The primary function of PEX19 is to act as a chaperone for peroxisomal membrane proteins, aiding in their delivery to the peroxisome. By utilizing PEX19 Gene Knockout Cell Lines, researchers can investigate the physiological implications of impaired peroxisomal function, which is linked to various metabolic disorders and genetic diseases such as Zellweger syndrome and other peroxisomal biogenesis disorders. These models enable scientists to elucidate the compensatory mechanisms cells may activate in response to PEX19 deficiency, adding significant depth to current understanding of peroxisomal dynamics.
In terms of scientific importance, the ability to study the PEX19 knockout phenotype allows for the exploration of therapeutic strategies aimed at correcting peroxisomal dysfunction. Compared to traditional cell line models, these knockout lines provide a more precise tool for dissecting genetic interactions and phenotypic outcomes, making them invaluable for both fundamental research and the development of targeted therapies.
What sets our PEX19 Gene Knockout Cell Lines apart is the rigorous validation and characterization process we employ, ensuring high specificity and reproducibility in experimental outcomes. Additionally, these cell lines come with a comprehensive support package that includes detailed protocols and potential applications, empowering researchers to advance their studies with confidence.
Our products are backed by a team of experts dedicated to biological research solutions, and we pride ourselves on delivering innovative tools that accelerate scientific discovery. PEX19 Gene Knockout Cell Lines represent a significant advancement in genomics and cell biology, cementing our commitment to excellence in the life sciences field.
Please note that all services are for research use only. Not intended for any clinical use.
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