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41 results about "Mononucleosis" patented technology

A disease usually caused by the Epstein-Barr virus (EBV).

Spring water monoucleosis for degrading alflatoxin B1 and ochratoxin A and application of spring water mononucleosis

ActiveCN105255776APromote degradationEfficient degradation and detoxification abilityBacteriaMicroorganism based processesMononucleosisAflatoxin B
The invention provides spring water monoucleosis for degrading alflatoxin B1 and ochratoxin A and application of the spring water mononucleosis and particularly provides a strain of difunctional efficient degrading bacteria (Silanimonas sp.) CW282 and application thereof in degrading low-pollution-concentration alflatoxin B1 and ochratoxin A. Compared with existing aflatoxin degrading bacteria, the strain CW282 can achieve excellent degrading effects under the condition of low-concentration toxin pollution. Under the condition of liquid fermentation, in a fermentation culture solution containing alflatoxin B1 and ochratoxin A with the final concentration being 20 micrograms per liter, the degrading rate of the strain CW282 on ochratoxin A is 70.7% in 24 h and reaches 95.6% in 48 h; the degrading rate of the strain CW282 on alflatoxin B1 is 86.9% in 24 h and reaches 91.3% in 48 h. When the strain CW282 is used for treating fodder (the final concentration is 20 micrograms per kg) polluted by toxins, the degrading rate on ochratoxin A is 53.2% in 48 h, and the degrading rate on alflatoxin B1 is 58.3% in 48 h. The strain CW282 has substantive application value and significance on the application aspects of food and feed biological detoxification.
Owner:CHACHA FOOD CO LTD

Multi-PCR detecting method capable of detecting mononuclear hyperplasia, staphylococcus aureus and enterococcus faecium simultaneously

The invention discloses a multi-PCR detecting method capable of detecting mononuclear hyperplasia, staphylococcus aureus and enterococcus faecium simultaneously. The multi-PCR detecting method capable of simultaneously detecting three pathogenic bacteria, namely, the mononuclear hyperplasia, the staphylococcus aureus and the enterococcus faecium, is established by designing premiers respectively according to the hlyA gene of the mononuclear hyperplasia, the NUC gene of the staphylococcus aureus and the ddl gene of the enterococcus faecium. According to the method, the DNA fragments of the mononuclear hyperplasia, the staphylococcus aureus and the enterococcus faecium can be amplified specifically; the lowest detecting amounts are 1.07 pg, 11.6 pg, and 1.21 pg respectively. The method does not have a cross reaction to other common pathogenic bacteria. The multi-PCR reaction established by the method has the characteristics of high specificity and high sensitivity; a convenient, quick and accurate method is provided for quick detection, authentication and epidemiological investigation of the mononuclear hyperplasia, the staphylococcus aureus and the enterococcus faecium in clinical work.
Owner:INNER MONGOLIA AUTONOMOUS REGION ACAD OF AGRI & ANIMAL HUSBANDRY SCI
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