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71 results about "Araliaceae" patented technology

The Araliaceae is a family made of 52 genera and 700 species of flowering plants including perennial herbs, trees, vines and succulents. The family has large, usually alternate leaves, five-petaled flowers arranged in clusters, and berries. Some genera, such as 'the ivies 'Hedera, are used as ornamental foliage plants, and the family also includes the Panax ginseng, the source of ginseng used in traditional Chinese medicine.

Wild ginseng and cultivated ginseng multiple polymerase chain reaction (PCR) test kit and identification method

The invention discloses a wild ginseng and cultivated ginseng multiple PCR test kit, which is characterized by containing: buffer solution, 12.5mM of deoxy-ribonucleoside triphosphate (dNTP), 0.1mM of one of a primer 1 and a primer 2, Taq DNA polymerase, a sample DNA to be tested and a double-distilled water identification reaction system; or the buffer solution, 12.5 mM of dNTP, 0.1 mM of one of the primer 1 and the primer 2, Taq DNA polymerase, wild ginseng and cultivated ginseng DNA 1:1 mixture and a double-distilled water positive reference reaction system; or the buffer solution, 12.5 mM of dNTP, 0.1 mM of one of the primer 1 and the primer 2, Taq DNA polymerase, araliaceae congeneric DNA 1:1 mixture, and a double-distilled water negative reference reaction system. The detection and identification method comprises the steps of designing two pairs of specific oligonucleotide primers of wild ginseng and cultivated ginseng mitochondrion DNAs, designing two pairs of specific oligonucleotide primers of synthetic wild ginseng and cultivated ginseng mitochondrion DNAs, determining a reaction process, determining result and the like. The method can accurately determine the specificity of both the wild ginseng and the cultivated ginseng, and the detection result is reliable.
Owner:BEIHUA UNIV

Method for removing propamocarb in araliaceae saponin extract

The invention discloses a method for removing propamocarb in araliaceae saponin extract. The method sequentially comprises the following steps that 1, the araliaceae saponin extract is taken and completely dissolved in water of 2-8 folds, an adsorption agent of 0.3%-0.8% fold is added, sedimentation is carried out after full stirring, and supernate is filtered; 2, an acetic acid test solution is slowly added dropwise to the supernate filtered in the step 1, the pH value is adjusted to range from 2 to 5, an organic solvent of 1 / 3 to 2 / 3 of the volume is added for extracting many times, the number of times of extracting ranges from 2 to 8, an organic phase is abandoned after an organic solvent is concentrated and recycled, and a water phase is collected; 3, the water phase obtained in the step 2 is taken to be concentrated and spray-dried or freeze-dried, and ginsenoside extract with propamocarb removed is obtained. According to the method, an adsorption-extraction combined method is adopted for gradually removing propamocarb pesticide residues in the araliaceae saponin extract according to the structure characteristics of propamocarb. By means of the technology, the existing residue removing efficiency is greatly improved, cost is reduced, and the method is suitable for mass production.
Owner:广东青云山药业有限公司

Traditional Chinese medicine preparation for treating gonitis and preparation method thereof

The invention belongs to the technical field of traditional Chinese medicines, and particularly relates to a traditional Chinese medicine preparation for treating gonitis and a preparation method thereof. The traditional Chinese medicine preparation for treating gonitis is prepared from the following raw materials in parts by weight: 10-50 parts of herba phrymae leptostachya, 5-60 parts of cortexerythrinae seu kalopanacis, 10-55 parts of caulis sinomenii, 5-55 parts of lignum phetimiae, 5-55 parts of radix euonymi hederacei, 5-50 parts of radix stephaniae tetrandrae, 10-90 parts of rhizoma saururi chinensis, 10-60 parts of radix araliaceae acanthopanax trifoliatus, 5-40 parts of radix et caulis ventilaginis leiocarpae, 10-40 parts of bark and leaf of saraca chinensis, 5-40 parts of radixtoddaliae asiaticae, 5-50 parts of rhizoma polygoni cuspidati, 5-40 parts of dragon's blood, 5-45 parts of ramulus et folium schefflerae leucanthae, 5-30 parts of herba daphniphylli, 5-30 parts of burmann cinnamon bark, 0.01-40 parts of radix fici simplicissimae and 0.01-40 parts of semen coicis. By adopting the traditional Chinese medicine preparation for treating a gonitis patient, a wind-cold-wetness evil which invades a body and extravasated blood and phlegm which block channels can be eliminated, and the traditional Chinese medicine preparation invigorates blood circulation, diminishes swelling, relaxes tendon, activates collaterals, promotes blood circulation of an affected part, dredges the channels and has a significant curing effect on gonitis.
Owner:GUANGXI UNIV OF CHINESE MEDICINE

Roxburgh rose and honey chestnut kernels and preparation method for same

The invention discloses roxburgh rose and honey chestnut kernels, which are prepared from the following raw materials: roxburgh roses, chestnuts, soybeans, loofahs, araliaceae acanthopanax trifoliatus, a proper amount of water, agaricus blazei murill, rosa davurica pall, verbenae herba, ginkgo leaves, mentha spicata, honey, Hailong oil and cordyceps militaris powder. A preparation method comprises the following steps: (1) preparing chestnut kernels for later use; (2) preparing mixed fruit and vegetable juice; (3) preparing cereal pulp; (4) preparing a nutrient solution; (5) preparing a soaking solution; (6) soaking the chestnut kernels for later use in the soaking solution, and after the chestnut kernels are tasty, fishing out and drying the chestnut kernels to obtain a finshed product. According to the roxburgh rose and honey chestnut kernels and the preparation method, fruit, vegetable and cereal nutrients such as the roxburgh roses and the araliaceae acanthopanax trifoliatus are introduced into the honey chestnut kernels, and meanwhile, beneficial healthcare components such as cordyceps militaris and the agaricus blazei murill are added, so that the honey chestnut kernels have a unique flavor, taste crispy and delicious, smell fruity, and have the healthcare effects of nourishing the stomach and spleen, invigorating the kidney, reinforcing tendons, promoting blood circulation, strengthening the body and the like, and nutritional substances required by a human body are supplemented.
Owner:安庆天然蜂坊蜂业有限公司

Tissue culture method for rapid propagation and seedling of Yunnan polygonatum kingianum tubers and stem tips

The invention discloses a tissue culture method for rapid propagation and seedling of Yunnan polygonatum kingianum tubers and stem tips. The tissue culture method comprises the following steps: 1) performing sterile germination of Yunnan polygonatum kingianum tubers and stem tips; 2) proliferation of Yunnan polygonatum kingianum protocorms; 3) performing differentiation of the Yunnan polygonatum kingianum protocorms; 4) strengthening seedlings of Yunnan polygonatum kingianum; 5) rooting large seedlings of Yunnan polygonatum kingianum. The tissue culture method has the advantages that by adjusting components of a seeding culture medium, Yunnan polygonatum kingianum tubers and stem tips seeded with the culture medium need no dark culture time but are subjected to direct light treatment, germinated seeds can form protocorms within about 14-25 days, and the germination rate is up to 96-98%; by adopting the tissue culture method, a very good promotion function is achieved for populations ofthe lily family medicinal plant in imminent danger, namely the Yunnan polygonatum kingianum, and a biological technique base is made for achievement of values of famous and precious traditional Chinese medicinal materials; bananas are adopted as a rooting culture medium preferably, the seedling time of the rooting culture medium with the bananas is 32-45 days, and the seedling time of a rooting culture medium with potatoes is 46-60 days.
Owner:临沧市云瑞堂生物科技有限公司

Thick soup with pickled cucumbers and Chinese chestnuts and making method of thick soup

The invention discloses thick soup with pickled cucumbers and Chinese chestnuts. The thick soup is made from raw materials including the pickled cucumbers, chestnut kernels, black millet, araliaceae acanthopanax trifoliatus, a moderate amount of water, raspberries, apple blossoms, sage, fresh bamboo leaves, dandelion, agar, maltitol and cordyceps militaris powder. The making method includes the steps of 1), making pickled-cucumber pulp; 2), making chestnut kernel pulp; 3), making black millet paste; 4), making vegetable juice; 5), making a nutrition solution; 6), soaking the agar prior to heating to be melt for standby use; 7), mixing the obtained materials, adding the maltitol, the cordyceps militaris powder and the water, boiling up with high-temperature fire, boiling out with soft fire and taking out of a pot till soluble solid reaches by 80-90% to obtain the product. Nutrient ingredients of the pickled cucumbers, the chestnut kernels, the araliaceae acanthopanax trifoliatus and the like are introduced into the thick soup, and meanwhile, beneficial elements of the raspberries, the cordyceps militaris powder and the like are added, so that nutritional value is improved; the thick soup is rich in taste, fresh and delicious in flavor and good in diet therapy and healthcare effect.
Owner:程序

Wild ginseng and cultivated ginseng multiple polymerase chain reaction (PCR) test kit and identification method

The invention discloses a wild ginseng and cultivated ginseng multiple PCR test kit, which is characterized by containing: buffer solution, 12.5mM of deoxy-ribonucleoside triphosphate (dNTP), 0.1mM of one of a primer 1 and a primer 2, Taq DNA polymerase, a sample DNA to be tested and a double-distilled water identification reaction system; or the buffer solution, 12.5 mM of dNTP, 0.1 mM of one of the primer 1 and the primer 2, Taq DNA polymerase, wild ginseng and cultivated ginseng DNA 1:1 mixture and a double-distilled water positive reference reaction system; or the buffer solution, 12.5 mM of dNTP, 0.1 mM of one of the primer 1 and the primer 2, Taq DNA polymerase, araliaceae congeneric DNA 1:1 mixture, and a double-distilled water negative reference reaction system. The detection and identification method comprises the steps of designing two pairs of specific oligonucleotide primers of wild ginseng and cultivated ginseng mitochondrion DNAs, designing two pairs of specific oligonucleotide primers of synthetic wild ginseng and cultivated ginseng mitochondrion DNAs, determining a reaction process, determining result and the like. The method can accurately determine the specificity of both the wild ginseng and the cultivated ginseng, and the detection result is reliable.
Owner:BEIHUA UNIV
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