Gene: PEX2
Official Full Name: peroxisomal biogenesis factor 2provided by HGNC
Gene Summary: This gene encodes an integral peroxisomal membrane protein required for peroxisome biogenesis. The protein is thought to be involved in peroxisomal matrix protein import. Mutations in this gene result in one form of Zellweger syndrome and infantile Refsum disease. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35753 | PEX2 Knockout cell line (HeLa) | Human | PEX2 | 1:3~1:6 | Negative | Online Inquiry |
KO35754 | PEX2 Knockout cell line (HCT 116) | Human | PEX2 | 1:2~1:4 | Negative | Online Inquiry |
KO35755 | PEX2 Knockout cell line (HEK293) | Human | PEX2 | 1:3~1:6 | Negative | Online Inquiry |
KO35756 | PEX2 Knockout cell line (A549) | Human | PEX2 | 1:3~1:4 | Negative | Online Inquiry |
PEX2 Gene Knockout Cell Lines are engineered cell models designed to facilitate the study of peroxisomal biogenesis and function by specifically disrupting the PEX2 gene. PEX2, a critical gene involved in the formation and maintenance of peroxisomes, plays a pivotal role in metabolic processes, including lipid metabolism and reactive oxygen species detoxification. By generating these knockout cell lines, researchers can observe the phenotypic consequences of PEX2 disruption, enabling a deeper understanding of diseases associated with peroxisomal dysfunction, such as Zellweger syndrome and other peroxisomal biogenesis disorders.
The cellular mechanisms underlying the function of PEX2 can be intricately explored through these knockout lines. Upon knockout of PEX2, researchers can evaluate the resulting impact on peroxisome biogenesis, protein import, and cellular metabolism. This provides invaluable insights into the specific roles that peroxisomes play in cellular homeostasis and their contributions to various metabolic pathways. The ability to manipulate and study genetic expression at this level is crucial in both basic research and therapeutic developments.
The scientific importance of PEX2 Gene Knockout Cell Lines extends to numerous applications, including pharmacological research, genetic disease modeling, and metabolic studies. These cell lines serve as powerful tools in drug discovery, allowing researchers to screen compounds that could restore peroxisomal function or to elucidate the mechanisms behind peroxisomal disorders.
What sets PEX2 Gene Knockout Cell Lines apart from other models is their specificity and reliability in mimicking the genetic landscape of human disease. Unlike traditional models, these knockout lines offer enhanced reproducibility and a more accurate representation of human pathology, making them indispensable in translational research.
Researchers and clinicians alike will find exceptional value in these cell lines, as they not only streamline experimental workflows but also significantly enhance the potential for novel therapeutic strategies targeting peroxisomal conditions. At [Your Company Name], our commitment to advancing scientific discovery is reflected in our precise engineering of these cell lines, backed by extensive expertise in genetic modifications and cellular biology.
Please note that all services are for research use only. Not intended for any clinical use.
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