Gene: PCSK5
Official Full Name: proprotein convertase subtilisin/kexin type 5provided by HGNC
Gene Summary: This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER. It then sorts to the trans-Golgi network where a second autocatalytic event takes place and the catalytic activity is acquired. This encoded protein is widely expressed and one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It mediates posttranslational endoproteolytic processing for several integrin alpha subunits and is thought to process prorenin, pro-membrane type-1 matrix metalloproteinase and HIV-1 glycoprotein gp160. Alternative splicing results in multiple transcript variants, some of which encode distinct isoforms, including a protease packaged into dense core granules (PC5A) and a type 1 membrane bound protease (PC5B). [provided by RefSeq, May 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO36182 | PCSK5 Knockout cell line (HCT 116) | Human | PCSK5 | 1:2~1:4 | Negative | Online Inquiry |
KO36183 | PCSK5 Knockout cell line (HEK293) | Human | PCSK5 | 1:3~1:6 | Negative | Online Inquiry |
KO36184 | PCSK5 Knockout cell line (A549) | Human | PCSK5 | 1:3~1:4 | Negative | Online Inquiry |
PCSK5 Gene Knockout Cell Lines refer to genetically engineered cell lines in which the proprotein convertase subtilisin/kexin type 5 (PCSK5) gene has been specifically disrupted. This classical knockout approach enables researchers to study the role of PCSK5 in various biological processes and pathologies. PCSK5 plays a significant role in the proteolytic processing of prohormones and is implicated in various disorders, including obesity, cardiovascular diseases, and metabolic syndromes. The mechanism of action for these knockout cell lines relies on the CRISPR-Cas9 gene editing technology, which creates targeted mutations leading to the complete absence of functional PCSK5 protein.
The scientific importance of PCSK5 Gene Knockout Cell Lines lies in their ability to facilitate detailed investigations into the regulatory mechanisms and pathways influenced by PCSK5. Researchers can employ these cell lines to explore the effects of PCSK5 deletion on cellular differentiation, metabolic pathways, and responses to hormonal signals. This enables a deeper understanding of the contributory role of PCSK5 in diseases and may pave the way for the development of targeted therapeutics.
One of the primary advantages of our PCSK5 Gene Knockout Cell Lines is their reliability and specificity, providing researchers with a robust model system that mimics the effects of complete gene loss in vivo. Unlike traditional RNA interference methods, which can lead to off-target effects, these knockout lines are designed to ensure a precise disruption of the PCSK5 gene, enhancing the reproducibility of experimental results. Furthermore, they come pre-validated for consistent performance across various assays, thereby streamlining the experimental process.
This product is particularly valuable to researchers in fields ranging from molecular biology to pharmacology, as it offers a unique tool for elucidating the intricate roles of proteases in physiological and pathological contexts. Clinicians focusing on metabolic diseases can also leverage these models for translational research aimed at identifying novel therapeutic targets.
Our company is dedicated to delivering high-quality biological products backed by extensive expertise in genetic engineering and cell biology. We ensure that our products meet rigorous standards for reliability and efficacy, making them an indispensable resource for advancing research in the life sciences.
Please note that all services are for research use only. Not intended for any clinical use.
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