Gene: PKD2
Official Full Name: polycystin 2, transient receptor potential cation channelprovided by HGNC
Gene Summary: This gene encodes a member of the polycystin protein family. The encoded protein is a multi-pass membrane protein that functions as a calcium permeable cation channel, and is involved in calcium transport and calcium signaling in renal epithelial cells. This protein interacts with polycystin 1, and they may be partners in a common signaling cascade involved in tubular morphogenesis. Mutations in this gene are associated with autosomal dominant polycystic kidney disease type 2. [provided by RefSeq, Mar 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
GP00401 | PKD2 gRNA1-gRNA2 KO plasmid | PKD2 | $850 | |||
KO00699 | PKD2 Knockout cell line(H1) | Human | PKD2 | 1:6-1:8 | Negative | Online Inquiry |
KO15102 | PKD2 Knockout cell line (HeLa) | Human | PKD2 | 1:3~1:6 | Negative | Online Inquiry |
KO15103 | PKD2 Knockout cell line (HCT 116) | Human | PKD2 | 1:2~1:4 | Negative | Online Inquiry |
KO15104 | PKD2 Knockout cell line (HEK293) | Human | PKD2 | 1:3~1:6 | Negative | Online Inquiry |
KO15105 | PKD2 Knockout cell line (A549) | Human | PKD2 | 1:3~1:4 | Negative | Online Inquiry |
PKD2 Gene Knockout Cell Lines are specialized cellular models engineered to lack the PKD2 gene, which encodes for the polycystin-2 protein involved in calcium homeostasis and cellular signaling. By eliminating the expression of PKD2, these cell lines serve as invaluable tools for investigating the pathophysiology of various diseases, particularly autosomal dominant polycystic kidney disease (ADPKD), a genetic disorder characterized by cyst formation in the kidneys and other organs.
The primary function of PKD2 Gene Knockout Cell Lines lies in their ability to facilitate the study of calcium signaling pathways and identify potential therapeutic targets for ADPKD and related disorders. These cell lines allow researchers to elucidate the consequences of PKD2 deficiency, including altered calcium influx, aberrant cellular proliferation, and increased susceptibility to apoptosis. By replicating the genetic conditions associated with ADPKD, scientists can assess the efficacy of gene therapies, pharmacological interventions, and other treatment modalities in a controlled environment.
The scientific importance of PKD2 Gene Knockout Cell Lines cannot be overstated, as they offer a unique platform for preclinical research and drug development. They can be utilized to screen potential therapeutics, develop biomarker-driven approaches, and conduct in-depth mechanistic studies, thereby accelerating the pace of discovery in renal pathobiology.
Compared to traditional cell lines that express functional PKD2, these knockout models provide enhanced specificity for studying the effects of PKD2 loss. Researchers benefit from more accurate models that recapitulate the human disease state, offering clearer insights into disease mechanisms and treatment responses. Additionally, the use of knockout technology allows for tailored experimentation, enhancing reproducibility and data integrity in experimental design.
For researchers and clinicians focused on understanding kidney diseases and exploring innovative treatments, PKD2 Gene Knockout Cell Lines represent a significant asset. Their customized nature and clear role in disease modeling empower scientists to make crucial advances in developing targeted therapeutics for conditions previously seen as challenging to treat.
As a leader in the field of genetic models, our company is dedicated to providing high-quality, precise biological products like PKD2 Gene Knockout Cell Lines to support cutting-edge research and therapeutic advancements. Our commitment to scientific excellence ensures that our offerings meet the rigorous demands of modern biomedical research.
Please note that all services are for research use only. Not intended for any clinical use.
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