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DDAH1 Knockout Cell Lines

Gene: DDAH1

Official Full Name: dimethylarginine dimethylaminohydrolase 1provided by HGNC

Gene Summary: This gene belongs to the dimethylarginine dimethylaminohydrolase (DDAH) gene family. The encoded enzyme plays a role in nitric oxide generation by regulating cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO29122 DDAH1 Knockout cell line (HeLa) Human DDAH1 1:3~1:6 Negative Online Inquiry
KO29123 DDAH1 Knockout cell line (HCT 116) Human DDAH1 1:2~1:4 Negative Online Inquiry
KO29124 DDAH1 Knockout cell line (HEK293) Human DDAH1 1:3~1:6 Negative Online Inquiry
KO29125 DDAH1 Knockout cell line (A549) Human DDAH1 1:3~1:4 Negative Online Inquiry

Background

DDAH1 Gene Knockout Cell Lines represent a vital tool in molecular and cellular biology, specifically designed to investigate the physiological roles of the DDAH1 gene. These cell lines have been meticulously engineered to disrupt the DDAH1 gene function, enabling researchers to study the downstream effects of this gene in various biological contexts. The DDAH1 gene encodes for the enzyme dimethylarginine dimethylaminohydrolase 1, which plays a significant role in regulating nitric oxide production and arginine metabolism, making it crucial for understanding vascular physiology and pathophysiology.

The primary function of these DDAH1 knockout cell lines lies in their ability to simulate the loss-of-function state associated with decreased nitric oxide bioavailability. This can significantly affect cellular signaling pathways, influencing factors such as cell proliferation, apoptosis, and inflammation. By employing these cell lines, scientists can elucidate the biological implications of diminished DDAH1 activity in various conditions, particularly in cardiovascular diseases, metabolic disorders, and organ transplantation.

In research and clinical settings, DDAH1 Gene Knockout Cell Lines serve as an essential resource for both basic research and drug development. They provide a model to identify novel therapeutic targets and screen potential drugs that can modulate DDAH1-related pathways. The genetic precision of these knockout models offers unparalleled specificity, allowing researchers to reliably attribute observed phenotypic changes to the absence of DDAH1 gene function.

Compared to traditional methods such as chemical inhibitors, DDAH1 Gene Knockout Cell Lines offer several advantages, including permanent and stable genetic modification that ensures consistent and reproducible results across experiments. Additionally, they circumvent potential off-target effects often associated with pharmacological treatments, making findings more robust and clinically translatable.

For researchers and clinicians investigating cardiovascular health or related metabolic pathways, DDAH1 Gene Knockout Cell Lines promise significant value, facilitating a deeper understanding of disease mechanisms and fostering innovation in therapeutic approaches. Our company takes pride in delivering high-quality genetic models backed by expert support, positioning us as a trusted partner in advancing biomedical research.

Please note that all services are for research use only. Not intended for any clinical use.

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