Gene: PRXL2C
Official Full Name: peroxiredoxin like 2Cprovided by HGNC
Gene Summary: Involved in positive regulation of ERK1 and ERK2 cascade and positive regulation of glycolytic process. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO14819 | PRXL2C Knockout cell line (HeLa) | Human | PRXL2C | 1:3~1:6 | Negative | Online Inquiry |
KO14820 | PRXL2C Knockout cell line (HCT 116) | Human | PRXL2C | 1:2~1:4 | Negative | Online Inquiry |
KO14821 | PRXL2C Knockout cell line (HEK293) | Human | PRXL2C | 1:3~1:6 | Negative | Online Inquiry |
KO14822 | PRXL2C Knockout cell line (A549) | Human | PRXL2C | 1:3~1:4 | Negative | Online Inquiry |
PRXL2C Gene Knockout Cell Lines are specifically engineered cellular models that have undergone the precise deletion of the PRXL2C gene, a gene implicated in various biological pathways, including those related to cellular stress responses and metabolic regulation. These knockout cell lines serve as invaluable tools for researchers aiming to explore the functional roles of the PRXL2C gene in both physiological and pathological contexts. By employing CRISPR-Cas9 technology or other gene-editing techniques, these cell lines are designed to elucidate the cellular mechanisms influenced by PRXL2C deficiency, thus providing insights into its contributions to diseases such as cancer and metabolic disorders.
The primary function of PRXL2C Gene Knockout Cell Lines is to facilitate the study of gene function through loss-of-function approaches. By utilizing these cell lines, researchers can conduct various assays to assess changes in cellular behavior, morphology, signaling pathways, and gene expression profiles as a direct result of PRXL2C disruption. This allows for a deeper understanding of how this gene modulates cellular processes and contributes to disease progression and overall organismal health.
In terms of scientific relevance, these knockout cell lines are crucial for advancing our understanding of molecular biology. They can be instrumental in drug discovery efforts, allowing scientists to identify potential therapeutic targets and investigate drug responses in an environment devoid of PRXL2C activity. Furthermore, these cell lines offer an experimental foundation for validating hypotheses related to gene function and interaction in a controlled setting, which is essential for progressing to higher-order physiological systems.
The advantages of using PRXL2C Gene Knockout Cell Lines over traditional models include their enhanced specificity and the precision of gene editing techniques that allow for exact deletions, minimizing off-target effects. Compared to cell lines that retain the PRXL2C gene, knockout lines provide an unambiguous framework to investigate the functions directly linked to the absence of this gene, making them more reliable for experimental replication and hypothesis testing.
For researchers and clinicians alike, the PRXL2C Gene Knockout Cell Lines represent a vital resource for advancing genetic research and therapeutic development. By plainly observing the phenotypic and molecular alterations resulting from gene knockout, users can derive rich data that may lead to breakthroughs in understanding disease mechanisms or discovering novel treatment avenues.
Our company prides itself on its commitment to providing high-quality biological products with cutting-edge technologies. With a dedicated team of experts in genetic engineering and cell biology, we strive to offer researchers robust and reliable tools, like PRXL2C Gene Knockout Cell Lines, that facilitate innovative research and contribute to scientific advancement.
Please note that all services are for research use only. Not intended for any clinical use.
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