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35 results about "Glycylglycine" patented technology

Glycylglycine is the dipeptide of glycine, making it the simplest peptide. The compound was first synthesized by Emil Fischer and Ernest Fourneau in 1901 by boiling 2,5-diketopiperazine (glycine anhydride) with hydrochloric acid. Shaking with alkali and other synthesis methods have been reported.

Anti-allergy face cream

InactiveCN108143638AExcellent emollientExcellent myogenicCosmetic preparationsToilet preparationsNaturally occurring surfactantsLanolin
The invention discloses anti-allergy face cream, and belongs to the technical field of daily chemicals. A method for preparing the anti-allergy face cream includes mixing sesame oil, natural surfactants and water with one another to obtain first mixtures and shearing the first mixtures at the high speed; sequentially adding ficus carica extract, cactaceae juice, glycylglycine, natural thickeners,honey, borneolum syntheticum, vegetable alkaloid, inositol, caffeine, carbomer and modified sepiolite into the first mixtures, stirring and mixing the ficus carica extract, the cactaceae juice, the glycylglycine, the natural thickeners, the honey, the borneolum syntheticum, the vegetable alkaloid, the inositol, the caffeine, the carbomer, the modified sepiolite and the first mixtures with one another and then carrying out high-pressure homogenization treatment, sterilization, discharging and filling to obtain the anti-allergy face cream. Ficus carica and water are smashed, pulped and filteredand then are mixed and boiled with natrii sulfas, and then cooling crystallization, filtering and drying are carried out to obtain the ficus carica extract; the natural surfactants comprise tea saponin, lecithin and lanolin; the natural thickeners comprise peach gum, xanthan gum and fucoidan. The anti-allergy face cream has the advantage that excellent anti-allergy effects can be realized by the anti-allergy face cream.
Owner:黄旭东

Seminal plasma gamma-L-glutamyl transpeptidase activity quantitative detecting reagent kit and application thereof

The invention discloses a seminal plasma gamma-L-glutamyl transpeptidase activity quantitative detecting reagent kit, which comprises a reagent R1 and a reagent R2; the reagent R1 comprises the following ingredients: 100 to 200 mmol / L trihydroxymethyl aminomethane buffer with pH value of 8.0 to 8.3, 90 to 110mmol / L glycylglycine and 0.01%to 0.1% antiseptic; and the reagent R2 comprises the following ingredients: 100 to 200mmol / L trihydroxymethyl aminomethane buffer with pH value of 8.0 to 8.3, 0.5 to 3.0mmol / L substrate and 0.01% to 0.1% antiseptic. The two liquid reagents can be directly used without being frozen at the temperature of minus 20 DEG C, the type and the consumption of the reagent can be remarkably reduced, and the sample is free from being diluted for more than 200 times; the substrate has good specificity and good appetency to the enzyme, so the reaction speed is fast; and the reagent kit is matched with an automatic biochemical instrument to use, so the procedures can be implified, the reagent can be saved, the manual error can be reduced, automatic and large-scale detection can be realized, the detection result is more accurate and more reliable, and the detection efficiency can be greatly improved.
Owner:南京欣迪生物药业工程有限责任公司

Firefly luciferase activity determination method

ActiveCN104946728AFacilitate high-throughput screeningEasy to useMicrobiological testing/measurementBiotinylationGlycylglycine
The invention belongs to the field of biological detection, and particularly relates to a firefly luciferase activity determination method. The method includes the following steps that mixed liquid containing ATP, Mn2+, Ca2+, fluorescein, aminolevulinic glycylglycine and phosphate is prepared; the PH value is adjusted; the mixed liquid is precooled to 4 DEG C; biotinylation luciferase is incubated in the mixed liquid; the ATP is added, the mixture is put into a detection instrument, and the intensity of a fluorescence signal is determined. By means of the determination method, high throughput screening and using of the luciferase are facilitated.
Owner:BEIJING ZHONGKEZIXIN TECH

Pore shrinking essence and preparation method thereof

The invention discloses pore shrinking essence and a preparation method thereof, and belongs to the technical field of essence. The pore shrinking essence is prepared from the following raw materialsin parts by weight: 2 to 4 parts of tea polyphenol extract, 2 to 4 parts of propolis extract, 1 to 3 parts of glycylglycine, 0.5 to 1 part of protease, 0.5 to 1 part of aminopeptidase, 1 to 2 parts ofchamomile extract, 1 to 2 parts of liquorice root extract, 1 to 3 parts of yeast polypeptide, 2 to 4 parts of fucus serratus extract, 1 to 3 parts of oliopeptide-20, 0.5 to 1 part of carbomer, 0.6 to2 parts of aminomethyl propanol, 3 to 6 parts of propanediol, 3 to 6 parts of 1,3-butanediol, 0.5 to 1 part of PEG (Polyethylene Glycol)-40 hydrogenated castor oil, 0.5 to 1 part of blumea balsamifera oil, 0.5 to 1 part of caprylin, 0.1 to 0.2 part of methyl hydroxybenzoate, 0.1 to 0.2 part of allantoin, 0.02 to 0.1 part of EDTA (Ethylene Diamine Tetraacetic Acid) disodium, 0.03 to 0.1 part of sodium hyaluronate and 70 to 100 parts of deionized water. Glycylglycine contains a component capable of inhibiting the adverse effect of unsaturated fatty acid, and is not only capable of shrinking anoutward spreading structure of pores, but also capable of improving the skin state surrounding the pores; the tea polyphenol is a water-soluble substance, and has the effects of cleaning the grease onthe face, astringing the pores, removing acne, diminishing inflammation and sterilizing.
Owner:WUHU YANGZHAN NEW MATERIAL TECH SERVICE CO LTD

Method for detecting activity of luciferase in sample

ActiveCN104975068AFacilitate high-throughput screeningEasy to useMicrobiological testing/measurementBiotinylationGlycylglycine
The invention relates to the field of biological detection, and in particular relates to a method for detecting activity of luciferase in a sample. The method comprises the step of incubating biotinylated luciferase in a mixed solution containing ATP, Mg<2+>, Ca<2+>, luciferin, amino acetyl glycylglycine and phosphate to generate optical signals. In the process of detecting the luciferase, the optical signal intensity is high, and the duration is long, so that the high-throughput screening and use of the luciferase are facilitated.
Owner:BEIJING ZHONGKEZIXIN TECH
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