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136 results about "Glycin" patented technology

Glycin, or N-(4-hydroxyphenyl)glycine, is N-substituted p-aminophenol. It is a photographic developing agent used in classic black-and-white developer solutions. It is unrelated to the amino acid glycine. It is typically characterized as thin plates of white or silvery powder, although aged samples appear brown. It is sparingly soluble in water and most organic solvents; it is readily soluble in alkalies and acids.

Method for producing chicken flavor essence base material by using chicken framework

The invention relates to a method for producing a chicken flavor essence base material by using a chicken framework, which comprises the following steps: firstly, crushing the cleaned chicken framework by a bone crusher, grinding the crushed chicken framework into chicken bone cement of which diameter is 10 +/- 5mu m by a colloid grinder, directly delivering the chicken bone cement into a reaction kettle without high-temperature boiling, adding water into the chicken bone cement to make the solid content reach 8 percent, and adjusting the pH to 7.0 by using 10 percent NaOH solution; adding 0.5 to 1.5 percent of composite proteinase by mass of the chicken bone cement into the mixture, and carrying out enzymolysis for 3 to 5 hours at a temperature of 55 DEG C; adding a thermal reaction mixture into the reaction kettle; heating the reaction kettle to make the mixture react at a temperature of between 100 and 125 DEG C; and after reacting for 30 to 180 minutes, obtaining the essence base material with intense chicken flavor, wherein the thermal reaction mixture comprises: 5 to 15 percent of glucose, 5 to 10 percent of xylose, 1 to 3 percent of cysteine hydrochloride, 1 to 3 percent of glycin, 30 to 50 percent of enzymolysis liquid, 1 to 5 percent of chicken fat, 5 to 20 percent of yeast powder, and 0.5 to 1.5 percent of vitamin B1.
Owner:TIANJIN UNIVERSITY OF SCIENCE AND TECHNOLOGY

Preparation process of intravenous injection human immunoglobulin

The invention relates to a preparation process of intravenous injection human immunoglobulin, belonging to the field of pharmaceuticals. On a basis of a traditional preparation process of intravenous injection human immunoglobulin with the low protein concentration of 5 percent, a filter pressing method is adopted instead of a centrifuging method in an extraction process. During hyperfiltration, the protein concentration is adjusted to 3-6 percent, a pH value is adjusted to 6.4-6.6 with 0.5 mol/L of NaOH; then, 1 mol/L phosphoric acid-NaOH buffer solution is added to adjust the electrical conductivity which is measured to be 0.175-0.205 s/m at a temperature T of 19 DEG C; and a chromatography method is adopted to carrying out column chromatography and purification by using upper ion exchange columns after the electrical conductivity is adjusted. The protein impurities can be effectively removed, the protein purify and the product yield are improved; maltose or glycin is used as a protector, which benefits the improvement of the stability of the intravenous injection human immunoglobulin; and the glycin is used as the protector, which satisfies the clinical use of diabetics. According to the invention, the intravenous injection human immunoglobulin with the protein concentration of 5-11 percent can be obtained.
Owner:华润博雅生物制药集团股份有限公司

Main field selenium-rich garlic pedicle, leaf, seed stalk and head cultivating method

The present invention discloses a planting method of the stem, leaf, bolt and head of field high-selenium garlic; the puke garlic of Cangshan is taken as the seed; people select field with more than 1.2 percent of organic material and implement disinsection treatment on soil seed before plantation; people strictly manage the field and apply selenium fertilizer made of aspartic acid, threonine, serine, glutamic acid, cysinic acid, glycin, arginine, total ammonia acid, nitrogen, phosphor, kalium, Na2SeO3, etc. on the leaf every other week. The selenium contents of the root, stem, leaf, bolt and head of the planted high-selenium garlic are separately between 21.75 and 35.83mg/kg, between 9.83and 20.12mg/kg, between 19.76 and 33.89mg/kg which are separately 311 times, 328 times and 725 times of that of the root, stem, leaf, bolt and head of garlic which are not added with selenium; the present invention is convenient for large-area field plantation and the root, stem, leaf, bolt and head of the planted high-selenium all contains active selenium which is beneficial to the health care of people; the raw material and extract can be used to make troche, capsule, injection, spray, oral liquid, health care food or commodity for hairdressing and skin protection integrating the functions of curing disease, health care and hairdressing.
Owner:蒋新东

Monoclonal antibodies to progastrin

The present invention provides progastrin-binding molecules specific for progastrin that do not bind gastrin-17(G17), gastrin-34(G34), glycine-extended gastrin-17(G17-Gly), or glycine-extended gastrin-34(G34-Gly). Further, the invention provides monoclonal antibodies (MAbs) selective for sequences at the N-terminus and the C-terminus of the gastrin precursor molecule, progastrin and the hybridomas that produce these MAbs. Also provided are panels of Mabs useful for the detection and quantitation of progastrin and gastrin hormone species in immuno-detection and quantitation assays. These assays are useful for diagnosing and monitoring a gastrin-promoted disease or condition, or for monitoring the progress of a course of therapy. The invention further provides solid phase assays including immunohistochemical (IHC) and immunofluorescence (IF) assays suitable for detection and visualization of gastrin species in solid samples, such as biopsy samples or tissue slices. The progastrin-binding molecules are useful therapeutically for passive immunization against progastrin in progastrin-promoted diseases or conditions. Also provided are surrogate reference standard (SRS) molecules that are peptide chains of from about 10 to about 35 amino acids, wherein the SRS molecule comprises at least two epitopes found in a protein of interest of greater than about 50 amino acids. Such SRS molecules are useful as standards in place of authentic proteins of interest.
Owner:CANCER ADVANCES INC

Method for preparing lanthanum subcarbonate nana-/micro-crystal by double hydrolysis regulation

The invention belongs to the micron-nanometer material preparation technique and the hydro-thermal synthesis technique field, in particular relates to a process for preparing a basic sodium lanthanum carbonate/micron crystal by means of double-hydrolytic regulation. The process has the specific steps that: a lanthanum oxide and an ammonium bicarbonate or a glycin being taken as precursors and a deionized water as a solvent are positioned in a hydrothermal reaction kettle in proportion, the mole ratio of the lanthanum oxide and the glycin or the ammonium bicarbonate is 1:20 to 1:45, and the added quantity of the deionized water is between 50 and 80 percent of the volume of a container; the hydrothermal reaction kettle provided with mixtures is put into a box-type resistance furnace for being heated to the temperature of between 150 and 220 DEG C, and the container is taken out after the 8 to 48h heating at such a temperature and is cooled naturally to the room temperature; and the needed product is obtained after washing and centrifugal separation. The preparing process has advantages of simple process, easy building of the whole preparing system, simple and convenient operation, easy control of conditions, low cost, easy control of the appearance and size of the product, high purity, good crystallinity and convenient and brief product treatment, and is applied to the mass industrial production.
Owner:TONGJI UNIV

Fermentation-method theabrownin preparation method

InactiveCN101455257ANot limited by production seasonEasy to controlTea extractionFood preparationGallic acid esterMoisture
A method for preparation of tea brown element using a fermentation method pertains to the field of processing technology. The method includes: A. comminuting the tea into 60-80 mesh, performing UV sterilization for 30min, adding deionized water, at the same time, adding saccharomycete or Aspergillus in the water, adding 1% of gallic acid or pyrogallic acid or glycin or glucose, standing for 60min, until using the food fresh keeping diaphragm to seal after the tea has fully absorbed the water; and then placing in the conditions of ventilation, temperature of 35-55 DEG C and humidity of 60-85%, for light-shading training for 20 days, to obtain the fermented tea with the tea brown element; B. the drying the fermented tea leaves dried at 60 DEG C to 10 percent moisture content, soaking for 30min in a solution with the feed liquid ratio of 1:50, filtering; extracting 100mL filtrate, adding 400mL edible alcohol, standing 3 hours after mixing, centrifugally filtrating, to obtain the crude extract of the tea brown element; and then using20% alcohol-water blend to dissolve the crude extract of the tea brown element, the obtained solution passing through the conventional concentrating and drying process to obtain the tea brown element. The present invention ahs advantages of easy control, fast velocity, high efficiency and no limitation of the producing seasons of tea leaves. efficient and not subject to seasonal restrictions on tea production advantages.
Owner:YUNNAN AGRICULTURAL UNIVERSITY
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