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GNOTHIS HOLDING SA ECUBLENS

Overview
  • Total Patents
    13
About

GNOTHIS HOLDING SA ECUBLENS has a total of 13 patent applications. Its first patent ever was published in 2000. It filed its patents most often in Germany. Its main competitors in its focus markets measurement, biotechnology and optics are GENALYTE INC, TSILIVAKOS VASSILIOS and KOKUSAI SHAKU KK.

Patent filings in countries

World map showing GNOTHIS HOLDING SA ECUBLENSs patent filings in countries
# Country Total Patents
#1 Germany 13

Patent filings per year

Chart showing GNOTHIS HOLDING SA ECUBLENSs patent filings per year from 1900 to 2020

Top inventors

# Name Total Patents
#1 Rigler Rudolf 10
#2 Korn Kerstin 3
#3 Edman Lars 2
#4 Serov Alexandre 1
#5 Goesch Michael 1
#6 Vogel Horst 1
#7 Winter Holger 1
#8 Popovic Radivoje 1
#9 Rochas Alexis 1
#10 Thyberg Per 1

Latest patents

Publication Filing date Title
DE10336080A1 Identification of luminescent molecules comprises fluorescence correlation spectroscopy
DE10326302A1 Bi-fluorophore-labeled probes for the detection of nucleic acids
DE10212960A1 Use of oxazine dyes as labeling groups for single molecule analysis
DE10211321A1 Use of capture probes for the detection of nucleic acids
DE10210737A1 Single-channel multi-color correlation analysis
DE10162536A1 Evanescence-based multiplex sequencing method
DE10162535A1 Sequencing across perforated membranes
DE10126083A1 Use of optical diffraction elements in detection methods
DE10115309A1 Microscope arrangement for fluorescence spectroscopy, in particular fluorescence correlation spectroscopy
DE10111420A1 To detect an analyte by fluorescence correlation spectroscopy, a set gap is established between the light focusing unit and the volume of the sample, and the sample carrier is thermally insulated from the light source
DE10103304A1 Process for fluorescence spectroscopic, in particular fluorescence correlation spectroscopic examination of a measurement sample and device for carrying it out
DE10065631A1 Characterizing nucleic acid polymorphisms, useful e.g. for detecting inherited disease, by extension of starter primer then single-molecule detection of incorporated nucleotide
DE10031842A1 Multiplex sequencing method