35 results about "Vitaceae" patented technology

Methods of prophylaxis or treatment of a disease state initiated by or characterized by platelet aggregation, that employ a fruit extract or active fraction thereof, are disclosed. In one embodiment, the fruit extract or active fraction thereof, is obtained from the fruit of plants of the families Solanaceae, Rutaceae, Cucurbitaceae, Rosaceae, Musaceae, Anacardiaceae, Bromeliaceae, Vitaceae, Arecaceae, Ericaceae and Lauraceae. Pharmaceutical compositions comprising a fruit extract or active fraction thereof having platelet aggregation inhibitory activity are also disclosed.

The invention relates to a production method of fermented vine tea, vine tea extract and vine tea drink. Tender stem leaves of ampelopsis humulifolia of vitaceae are taken as raw material, fermentation technique is adopted for production, and the production method comprises the steps of preparing vine tea, wetting the vine tea by adding water and steaming; preparing a seed culture medium, autoclaving, cooling, then inoculating edible funguses, and culturing at 28-40 DEG C for 24-120 hours to obtain seeds; inoculating seeds at the ratio of 3-8% of the weight of the vine tea, fermenting at 28-40 DEG C for more than 120 hours, and drying to obtain the fermented vine tea; and extracting, concentrating and drying to obtain fermented vine tea powder. The edible funguses in the invention comprise aspergillus niger, aspergillus oryzae, monacus anka, saccharomycetes, lactic acid bacteria and mixed strains. In the fermentation process of the vine tea in the invention, contents of active ingredients such as soluble flavone, polyphenol, tea pigment and the like are greatly improved, thus promoting absorption and utilization of the active ingredient of the vine tea and enhancing pharmacological efficacy of the vine tea. Besides, the production process of the invention thoroughly solves the technical problem that vine tea soup is precipitated after being cooled.

Disclosed is an activity enhancer for oxidized protein hydrolase. The activity enhancer for oxidized protein hydrolase is characterized by comprising an extract of at least one plant selected from the group consisting of plants belonging to Compositae Anthemis (Chamaemelum), Saururaceae Houttuynia, Rosaceae Crataegus and Vitaceae Vitis. It is preferable that the activity enhancer for oxidized protein hydrolase comprises an extract of a plant belonging to Compositae Anthemis (Chamaemelum), an extract of a plant belonging to Saururaceae Houttuynia, an extract of a plant belonging to Rosaceae Crataegus and an extract of a plant belonging to Vitaceae Vitis. It is also preferable that the plant belonging to Compositae Anthemis (Chamaemelum) is Anthemis nobilis L., the plant belonging to Saururaceae Houttuynia is Houttuynia cordata Thunberg, the plant belonging to Rosaceae Crataegus is Crataegus oxyacantha L. and the plant belonging to Vitaceae Vitis is Vitis vinifera L.

The invention relates to a universal SNP typing probe in gramineous plants. The probe is composed of two pairs of reverse complement oligonucleotide sequences, and a fluorescence reporter group and a fluorescence quenching group are respectively positioned in reverse complement oligonucleotide chains. A present Taqman probe method is improved to design the SNP typing universal Taqman probe, so the experiment cost is reduced, and a Taqman probe SNP typing method can be widely applied in SNP detection of the gramineous plants.

The invention provides PCR (polymerase chain reaction) primers, method and kit for analyzing genetic diversity in gramineous plants. According to the technical scheme provided herein, 3 DNA templates different in character are picked from 13 DNA parts, 21 pairs of primers with clear polymorphic bands are screened out of 100 pairs of primers, the 21 pairs of primers are used to mark the 13 DNA parts, electrophoresis, imaging, photographing and data statistics are performed, UPGMA (unweighted pair-group method with arithmetic means) cluster analysis is performed on genetic similarity and genetic distances of the plants, and diversity analysis and interspecific relation research are performed. The research indicates that gramineous plant germplasm resources show rich genetic diversity; the genetic groups of these materials have no great relationship with geographic origin and geographic environment; SRAP (sequence-related amplified molecular polymorphism) marker is a molecular marker suitable for the research on gramineous plant germplasm resources.