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333 results about "Kinetin" patented technology

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Kinetin (/'kaɪnɪtɪn/) is a type of cytokinin, a class of plant hormone that promotes cell division. Kinetin was originally isolated by Miller and Skoog et al. as a compound from autoclaved herring sperm DNA that had cell division-promoting activity. It was given the name kinetin because of its ability to induce cell division, provided that auxin was present in the medium. Kinetin is often used in plant tissue culture for inducing formation of callus (in conjunction with auxin) and to regenerate shoot tissues from callus (with lower auxin concentration).

Personal care compositions and methods for the beautification of mammalian skin and hair

InactiveUS20070009474A1BiocideCosmetic preparationsPersonal careAdditive ingredient

Personal care composition comprising from about 0.05% to about 5% of at least one aquaporin-stimulating compound selected from the group consisting of xanthine, caffeine; 2-amino-6-methyl-mercaptopurine; 1-methyl xanthine; 2-aminopurine; theophylline; theobromine; adenine; adenosine; kinetin; p-chlorophenoxyacetic acid; 2,4-dichlorophenoxyacetic acid; indole-3-butyric acid; indole-3-acetic acid methyl ester; beta-naphthoxyacetic acid; 2,3,5-triiodobenzoic acid; adenine hemisulfate; n-benzyl-9-(2-tetrahydropyranyl)adenine; 1,3-diphenylurea; 1-phenyl-3-(1,2,3-thiadiazol-5-yl)urea; zeatin; indole-3-acetic acid; 6-benzylaminopurine; alpha-napthaleneacetic acid; 6-2-furoylaminopurine; green tea extract; white tea extract; menthol; tea tree oil; ginsenoside-RB1; ginsenoside-RB3; ginsenoside-RC; ginsenoside-RD; ginsenoside-RE; ginsenoside-RG1; ginseng root extract; ginseng flower extract; pomegranate extract, extracts from Ajuga turkestanica; extracts from viola tricolor and combinations thereof; an additional ingredient selected from the group consisting of niacinamide, glycerin and mixtures thereof, and a dermatologically-acceptable carrier.

Owner:THE PROCTER & GAMBLE COMPANY

Plant sprouting agent and preparation method thereof

ActiveCN102511488APromote division and differentiationActivate vitalityBiocidePlant growth regulatorsBiotechnologyPlant stem

The invention relates to a plant sprouting agent and a preparation method thereof. The materials of the sprouting agent are 6-benzyladenine, kinetin, gibberellin, dimethylsulfoxide, glycerol and lanolin; the dimethylsulfoxide solution and the glycerol are added into a glass beaker and dissolved, so that hormone solution is obtained; the lanolin is put into another big beaker, and is heated to 70 DEG C to be melted, and as the lanolin is stirred to be slowly melted, the hormone solution is slowly added into the lanolin and sufficiently and uniformly stirred; and after being cooled to the room temperature, the hormone mixture is coagulated into paste, which is the high-effective plant sprouting agent. Each component in the sprouting agent can rapidly penetrate the cell membranes of the dormant buds of plants and directionally enter cells, consequently, the efficacy is enhanced, and the acting time is shortened. The plant sprouting agent can increase the plant sprouting speed, shorten the growing time and accelerate seedling formation; bud dormancy is broken, so that the growth of plants is increased; the plant sprouting agent can change the hormonal balance in plant cells, promote sprouting and accelerate the elongation growth of the stems and leaves of plants; and the plant sprouting agent has a moisture-keeping effect, which can help to protect the new sprouts of plants.

Owner:HENAN UNIV OF SCI & TECH

Tender stem callus plant regeneration induction culture medium for lonicera caerulea

InactiveCN102119657APromote healthy growthPromote productionPlant tissue cultureHorticulture methodsAxillary budCalla

The invention relates to a tender stem callus plant regeneration induction culture medium for lonicera caerulea and solves the problems of low plant differentiation rate and high culture medium cost problem of the auxiliary bud or stem tip culture, which is the main tissue culture of lonicera caerulea. The culture medium consists of a large amount of macroelements, microelements and hormone, wherein the hormone consists of 6-benzyl aminopurine at a concentration of 1.0 to 2.0mg / L and indolebutyric acid or naphthylacetic acid at a concentration of 0.05 to 0.2mg. When the LD1 culture medium of the invention is used, the tender stems of lonicera caerulea can be easily induced to form calla, and the induction rates of the calla are all over 90 percent; and the probability of the induction of the calla into plants is high, the plant differentiation rate is up to 50 to 82 percent which is 66.6 to 173.3 percent higher than that of the conventional Murashige-Skoog (MS) culture medium, and the cost is saved by 45.1 percent compared with the reference MS culture medium.

Owner:NORTHEAST INST OF GEOGRAPHY & AGRIECOLOGY C A S

Efficient tissue culture and rapid propagation technology for seedlings of bletilla striata

ActiveCN105145352AMature technologyPerfect systemPlant tissue cultureHorticulture methodsBletilla striataSucrose

The invention discloses an efficient tissue culture and rapid propagation technology for seedlings of bletilla striata. According to the technology, bletilla striata seeds are sown on a seed germination culture medium for sterile germination, the obtained seedlings are inoculated to a multiplication and subculture medium one by one for multiplication and subculture, clustering seedlings are obtained and inoculated to a rooting culture medium for rooting culture, the obtained tissue culture seedlings are planted on a prepared seedling hardening substrate, and the seedlings are transplanted to a large filed for plantation after seedling hardening, wherein the seed germination culture medium comprises MS (magnesium sulfate), 30g / L of sugar, 8g / L of agar and 10g / L-12g / L of potatoes; the multiplication and subculture medium comprises MS, 1.0 mg / L of KT (kinetin), 0.2 mg / L of NAA (naphthalene acetic acid), 30g / L of sugar and 9g / L of agar; the rooting culture medium comprises MS, 0.2 mg / L of NAA, 1.0mg / L of IAA (indole acetic acid), 30g / L of sugar, 9g / L of agar and 25-30 g / L of potatoes; the seedling hardening substrate comprises medium moor peat soil, perlite and wood dust in the volume ratio being 5:2:3. The technology is mature, a system is perfect, the problems of low natural germination rate of bletilla striata and difficulty in obtaining of seedlings can be effectively solved, and the technology has better popularization and application value and broad market prospect.

333 results about "Kinetin" patented technology

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