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2931results about How to "High luminous intensity" patented technology

Full spectrum sunshine simulation apparatus for developing biological growth

Disclosed is a full spectrum sunshine simulation apparatus for developing biological growth which comprises a full spectrum light emitting diode module and a photoperiod controller. Therein, the full spectrum light emitting diode module includes a printed circuit board and a plurality of full spectrum light emitting diodes, wherein the luminescence spectrum of the full spectrum light emitting diodes has a wavelength range of 350 nm to 800 nm. The photoperiod controller, connected to the full spectrum light emitting diode module, is in charge of lighting periods of the plurality of full spectrum light emitting diodes, color temperatures and emitting angles of the lights emitted from the plurality of full spectrum light emitting diodes, thereby simulating a environment under artificial sunlight.
Owner:SINETICS ASSOCS INT TAIWAN +1

Method for highly sensitive quantitative detection of quantum dot fluorescence immunochromatographic assay

ActiveCN102520165ASensitive quantitative detection fastRealize detectionMaterial analysisCritical illnessLinear range
The invention discloses a method for highly sensitive quantitative detection of quantum dot fluorescence immunochromatographic assay. The method includes: building a fluorescence immunochromatographic assay test strip on the basis of optimizing the structure of the test strip and components by the aid of excellent fluorescent characteristics of quantum dots and by means of combining quantum dot fluorescence labeling technology and immunochromatographic assay; detecting fluorescence signal strength of a quantitative belt and a quality control belt by the aid of a fluorescence quantometer and correcting the fluorescence strength of the quantitative belt by the aid of the quality control belt after immunochromatographic assay of the test strip; and further quantitatively detecting analyte according to a standard curve obtained by the fluorescence quantometer. The method is simple, rapid, accurate, low in cost and quite high in sensitivity. Compared with a conventional colloidal gold immunochromatographic assay method, the method has the advantages of fine labeling stability, low non-specificity, high sensitivity, wide linear range and accuracy in quantization. The method is applicable to samples such as blood samples, urine samples, spittle, excrement and the like, and can be applied to detection of critical illness, poison, food safety and the like.
Owner:BEIJING KANGMEI TIANHONG BIOTECH

Broad-spectrum A1(1-x-y)InyGaxN light emitting diodes and solid state white light emitting devices

A broad-spectrum Al(1-x-y)InyGaxN light emitting diode (LED), including: a substrate, a buffer layer, an N-type cladding layer, at least one quantum dot emitting layer, and a P-type cladding layer. The buffer layer is disposed over the substrate. The N-type cladding layer is disposed over the buffer layer to supply electrons. The quantum dot emitting layer is disposed over the N-type cladding layer and includes plural quantum dots. The dimensions and indium content of the quantum dots are manipulated to result in uneven distribution of character distribution of the quantum dots so as to increase the FWHM of the emission wavelength of the quantum dot emitting layer. The P-type cladding layer is disposed over the quantum dot emitting layer to supply holes. A broad-spectrum Al(1-x-y)InyGaxN yellow LED may thus be made from the LED structure of this invention, with an emission wavelength at maximum luminous intensity falling within a range of 530˜600 nm, and FWHM within a range of 20˜150 nm. After packaging an Al(1-x-y)InyGaxN blue LED to form a solid state white light emitting device, the mixing of blue light and yellow light would generate white light with a high CRI index, high luminous intensity and capable of various color temperature modulation.
Owner:GENESIS PHOTONICS

Nitrogen-doped high-luminescent carbon quantum dot and preparation method thereof

The invention provides a nitrogen-doped high-luminescent carbon quantum dot and a preparation method thereof. The preparation method comprises the following steps: reacting by using a sodium citrate solution as a carbon source and ethanediamine as a source of N under a sealing condition, cooling an obtained product, then separating, and drying a solution obtained after separation so as to obtain the nitrogen-doped high-luminescent carbon quantum dot. The preparation method is simple in process, short in preparation period, low in manufacturing cost and good in repeatability; obtained raw materials are simple and easily available. The nitrogen-doped high-luminescent carbon quantum dot prepared by using the method is uniform in size distribution and high in luminescent density; the luminescent density of the nitrogen-doped high-luminescent carbon quantum dot is about 20 times of that of a general quantum dot, so that the application of the nitrogen-doped high-luminescent carbon quantum dot in the field of cell marking can be expanded. As the improvement of the luminescent density is caused by nitrogen doping, the nitrogen-doped high-luminescent carbon quantum dot prepared by the method has unique application when being used for detecting whether N exists in environments.
Owner:CHINA UNIV OF PETROLEUM (BEIJING)

Fluorescence immunochromatographic assay and kit for quantitative detection of troponin I/creatine kinase isoenzyme/myohemoglobin

The invention discloses a quantum dot multicolor marking method for quantitative detection of various cardiovascular disease markers and a kit of troponin I / creatine kinase isoenzyme / myohemoglobin. The method realizes fluorescent quantitative detection by utilizing excellent fluorescent properties of quantum dots and combining a multicolour marking technology and an immunochromatographic assay on the basis of optimizing each component of a test strip. Compared with the common collaurum immunochromatographic assay, the method has the advantages of good mark stability, low nonspecificity, high sensitivity, wide linear range, small cross interference, and accuracy in quantification. The kit disclosed by the invention is used for carrying out quantification detection on the troponin I, the creatine kinase isoenzyme and the myohemoglobin simultaneously, is suitable for detection of whole blood, blood serum and plasma samples, can provide a reference for cardiovascular and cerebrovascular disease diagnosis, and is widely applied to primary hospitals and clinics.
Owner:SHENZHEN KANGMEI BIOTECH
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