Gene: PIEZO1
Official Full Name: piezo type mechanosensitive ion channel component 1 (Er blood group)provided by HGNC
Gene Summary: The protein encoded by this gene is a mechanically-activated ion channel that links mechanical forces to biological signals. The encoded protein contains 36 transmembrane domains and functions as a homotetramer. Defects in this gene have been associated with dehydrated hereditary stomatocytosis. [provided by RefSeq, Jul 2015]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00896 | PIEZO1 Knockout cell line(HT-29) | Human | PIEZO1 | 1:2~1:4 | Negative | Online Inquiry |
KO00915 | PIEZO1 Knockout cell line(BEAS-2B) | Human | PIEZO1 | 1:3~1:4 | Negative | Online Inquiry |
KO01434 | PIEZO1 Knockout cell line (293T) | Human | PIEZO1 | 1:3~1:6 | Negative | Online Inquiry |
KO15147 | PIEZO1 Knockout cell line (HeLa) | Human | PIEZO1 | 1:3~1:6 | Negative | Online Inquiry |
KO15148 | PIEZO1 Knockout cell line (HCT 116) | Human | PIEZO1 | 1:2~1:4 | Negative | Online Inquiry |
KO15149 | PIEZO1 Knockout cell line (HEK293) | Human | PIEZO1 | 1:3~1:6 | Negative | Online Inquiry |
KO15150 | PIEZO1 Knockout cell line (A549) | Human | PIEZO1 | 1:3~1:4 | Negative | Online Inquiry |
PIEZO1 Gene Knockout Cell Lines are engineered cellular models designed specifically to explore the functional roles of the PIEZO1 gene, which encodes a mechanosensitive ion channel involved in various physiological processes, including touch sensation, blood pressure regulation, and cell signaling. By creating these knockout cell lines, researchers can eliminate PIEZO1 expression, allowing for the examination of downstream effects and mechanisms that are critical for understanding both normal physiology and pathological conditions.
The primary function of these cell lines is to allow scientists to investigate the PIEZO1 pathway's contributions to mechanotransduction—the process by which cells convert mechanical stimuli into electrical or biochemical signals. Through advanced techniques such as CRISPR/Cas9 gene editing, PIEZO1 expression is effectively disrupted, enabling researchers to conduct experiments assessing changes in cellular responses to mechanical stress, ion flux, and other cellular behaviors.
The scientific importance of PIEZO1 Gene Knockout Cell Lines extends to a wide array of applications in both research and clinical settings. These cell lines are invaluable in studies related to cardiovascular health, developmental biology, and pain mechanisms, contributing to our understanding of diseases like hypertension, osteoarthritis, and even sensory impairments. Researchers are increasingly recognizing the relevance of mechanosensitive channels in various therapeutic contexts, making these knockout models central to advancing knowledge and potential treatment strategies.
One of the distinctive advantages of our PIEZO1 Gene Knockout Cell Lines is their precise gene editing, which allows for a clean and complete knockout without the risk of off-target effects commonly associated with older gene silencing techniques. This specificity enhances reproducibility and reliability in experimental outcomes, making it a preferred choice for scientists seeking to yield substantive insights.
For researchers and clinicians focused on dissecting the complex pathways linked to mechanotransduction and cellular responses, these knockout cell lines present a robust toolset. The clarity and reliability of results obtained from these models can significantly accelerate the pathway to impactful discoveries and innovative therapies.
Our company is committed to providing high-quality biological products characterized by scientific robustness and innovative design. With expertise in genetic engineering and a strong background in cell line development, we are dedicated to supporting the scientific community's efforts to unlock the complexities of cellular biology and improve human health outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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