Identification of novel phytocannabinoids from Ganoderma by label-free dynamic mass redistribution assay

2020 ◽  
Vol 246 ◽  
pp. 112218 ◽  
Author(s):  
Han Zhou ◽  
Xingrong Peng ◽  
Tao Hou ◽  
Nan Zhao ◽  
Minghua Qiu ◽  
...  
Keyword(s):  
Label Free ◽  
Dynamic Mass ◽  
Mass Redistribution ◽  
Free Dynamic

Applying label-free dynamic mass redistribution technology to frame signaling of G protein–coupled receptors noninvasively in living cells

2011 ◽  
Vol 6 (11) ◽  
pp. 1748-1760 ◽  
Author(s):  
Ralf Schröder ◽  
Johannes Schmidt ◽  
Stefanie Blättermann ◽  
Lucas Peters ◽  
Nicole Janssen ◽  
...  
Keyword(s):  
G Protein ◽  
Living Cells ◽  
G Protein Coupled Receptors ◽  
Label Free ◽  
Dynamic Mass ◽  
Mass Redistribution ◽  
G Protein Coupled ◽  
Free Dynamic

Applying label-free dynamic mass redistribution assay for studying endogenous FPR1 receptor signalling in human neutrophils

2017 ◽  
Vol 88 ◽  
pp. 72-78 ◽  
Author(s):  
Hanna B. Christensen ◽  
David E. Gloriam ◽  
Daniel Sejer Pedersen ◽  
Jack B. Cowland ◽  
Niels Borregaard ◽  
...  
Keyword(s):  
Human Neutrophils ◽  
Label Free ◽  
Dynamic Mass ◽  
Receptor Signalling ◽  
Mass Redistribution ◽  
Free Dynamic

Phenotypic assessment and ligand screening of ETA/ETB receptors with label-free dynamic mass redistribution assay

2019 ◽  
Vol 393 (6) ◽  
pp. 937-950
Author(s):  
Lala Qu ◽  
Xiuli Zhang ◽  
Jixia Wang ◽  
Han Zhou ◽  
Tao Hou ◽  
...  
Keyword(s):  
Label Free ◽  
Dynamic Mass ◽  
Ligand Screening ◽  
Mass Redistribution ◽  
Free Dynamic

scholarly journals A label-free screening approach targeted protease-activated receptor 1 based on dynamic mass redistribution in living cells

RSC Advances ◽  
2017 ◽  
Vol 7 (68) ◽  
pp. 43005-43013 ◽  
Author(s):  
Weiwei Tang ◽  
Bixia Huang ◽  
Jiancheng Wang ◽  
Lin An ◽  
Huailing Zhong ◽  
...  
Keyword(s):  
Platelet Aggregation ◽  
Living Cells ◽  
Label Free ◽  
Dynamic Mass ◽  
Screening Approach ◽  
Mass Redistribution ◽  
Protease Activated Receptor 1

Protease-activated receptor 1 (PAR-1) antagonists strongly inhibit thrombin-induced platelet aggregation and are proved to be effective as anti-thrombotic drugs.

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