Gene: PCCA
Official Full Name: propionyl-CoA carboxylase subunit alphaprovided by HGNC
Gene Summary: The protein encoded by this gene is the alpha subunit of the heterodimeric mitochondrial enzyme Propionyl-CoA carboxylase. PCCA encodes the biotin-binding region of this enzyme. Mutations in either PCCA or PCCB (encoding the beta subunit) lead to an enzyme deficiency resulting in propionic acidemia. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
GP01100 | PCCA gRNA5-gRNA6 KO plasmid | PCCA | $850 | |||
KO00388 | PCCA Knockout cell line(Hep G2) | Human | PCCA | 1:2~1:4 | Negative | Online Inquiry |
KO00862 | PCCA Knockout cell line(HeLa) | Human | PCCA | 1:3~1:6 | Negative | Online Inquiry |
KO15317 | PCCA Knockout cell line (HCT 116) | Human | PCCA | 1:2~1:4 | Negative | Online Inquiry |
KO15318 | PCCA Knockout cell line (HEK293) | Human | PCCA | 1:3~1:6 | Negative | Online Inquiry |
KO15319 | PCCA Knockout cell line (A549) | Human | PCCA | 1:3~1:4 | Negative | Online Inquiry |
PCCA Gene Knockout Cell Lines are specialized genetically modified cell lines designed to facilitate studies of the PCCA gene, which plays a critical role in human metabolism, particularly in the metabolism of branched-chain amino acids. These cell lines are engineered using advanced CRISPR-Cas9 technology to create precise knockouts of the PCCA gene, allowing researchers to explore the physiological impacts of PCCA deficiency and its association with metabolic disorders such as propionic acidemia.
The key function of PCCA Gene Knockout Cell Lines lies in their ability to model and mimic the phenotypic effects of PCCA mutations. Through the ablation of the target gene, these cell lines enable the examination of downstream metabolic pathways, cellular responses, and compensation mechanisms. Researchers can employ this tool for high-throughput drug screening, investigating potential therapeutic candidates, or deciphering the genetics of complex diseases related to metabolic dysfunction.
Scientifically, the PCCA Gene Knockout Cell Lines represent a valuable asset in both basic and translational research. They facilitate a deeper understanding of metabolic pathways and their genetic regulation, critical for developing innovative treatments for metabolic disorders. Moreover, the ability to simulate PCCA-related diseases in vitro provides a practical approach for elucidating disease mechanisms and developing personalized medicine strategies.
Compared to alternative models, such as wild-type or less specifically engineered cell lines, our PCCA Gene Knockout Cell Lines offer unprecedented specificity and reproducibility, ensuring that experimental results are directly attributable to the knockout of the PCCA gene. This advantage enhances experimental reliability and improves research outcomes, making it an indispensable tool in the resource toolkit of researchers and clinicians alike.
Investing in PCCA Gene Knockout Cell Lines can significantly accelerate your research endeavors, contributing to the advancement of knowledge in metabolic genetics and paving the way for future therapeutic innovations. In addition, our company boasts a strong commitment to excellence in genetic tools, providing you with products backed by rigorous development processes and comprehensive support.
Please note that all services are for research use only. Not intended for any clinical use.
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