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37 results about "Rabbit brain" patented technology

Prothrombin time test kit and preparation method thereof

A prothrombin time test kit consists of thromboplastin and a buffer liquid system, wherein the thromboplastin is rabbit brain tissue factors and recombinant tissue factors. The buffer liquid system comprises 30-50mM Tris-HCL, 3-10% of glycine, 1-5% of bovine serum albumin, 0.6-1.3% of sodium chloride, 6.8-8.4mM of calcium chloride and 30.5% of NaN, and the pH value of the buffer liquid system is 6.0-8.0. The thromboplastin also comprises rabbit cephalin. According to the invention, the defects that the sensitiveness indexes of various instruments are different due to the differences of the methods of the different instruments can be overcome, the high-sensitivity human recombinant thromboplastin and low-sensitivity rabbit brain powder extracting thromboplastin are combined, the PT reagent capable of meeting different methods of coagulometer can be prepared according to certain proportion, and the ISI (insulin sensitivity index) value is close to 1.0. The invention also discloses a preparation method of the prothrombin time test kit simultaneously.
Owner:武汉塞力斯生物技术有限公司

Hepaplastin test determination kit and preparation method thereof

InactiveCN105372424AImprove stabilityImprove accuracyMaterial analysisTissue factorBlood Coagulation Factor VII
The invention discloses a hepaplastin test determination kit and a preparation method thereof. Through combination of a buffer solution system a containing multiple effective components, plasma without blood coagulation factors VII, II, X and IX, a buffer system b, rabbit brain powder and tissue factor ester, the hepaplastin test determination kit improves reagent stability. A hepaplastin test determination reagent with good accuracy, good repeatability and good effects is further obtained.
Owner:WUHAN KING DIAGNOSTIC TECH CO LTD

Preparation method for rabbit brain tissue factor freeze-drying preparation

The invention discloses a preparation method for a rabbit brain tissue factor freeze-drying preparation. The preparation method comprises the following steps: taking a fresh rabbit brain and stripping meninx and blood vessels; removing a brainstem and washing by using normal saline; putting the rabbit brain into a cleaning mortar and adding acetone until the rabbit brain is immersed; grinding by using a grinding hammer and pouring off the acetone; repeating for three times; filtering the acetone by using filtering paper; putting the rabbit brain into an oven of 37 DEG C and paving to evaporate and dry the acetone; adding the normal saline; uniformly agitating and putting a mixture into a constant-temperature water bath of 37 DEG C to be pre-heated and activated, incubated and agitated; centrifuging for separating; taking liquid supernatant and filtering to obtain a rabbit brain FIII tissue factor suspension solution; adding the rabbit brain FIII tissue factor suspension solution into a small bottle; freezing-drying, exhausting and pressing a bottle to prepare the rabbit brain tissue factor freeze-drying preparation, and storing at -20 DEG C. With the adoption of the scheme, the technology is very mature, the quality is very stable and the guarantee period is very long; the preparation method is very convenient to use; the preparation method has very high medical teaching, scientific research, clinical diagnosis and treatment and economic values.
Owner:WANNAN MEDICAL COLLEGE

Egg-laying bird feedstuff additive

The invention relates to an egg laying poultry feed additive for supplying and adding a dietary factor. The constituents and the weight percentages thereof are as follows: soy protein bioactive peptides powder 25-30%, allium mongolicum powder 15-20%, sunflower seed powder 2%-5%, linseed 3%-5%, hemp seed powder 3%-5%, rabbit brain powder 5%-10%, perillaseed powder 5%-10%, black sesame seed powder 5%-10%, parslane herb powder 5%-10%, brown sugar 5%-10%, chicken's gizzard-membrane powder 2%-5%, dried orange peel powder 3%-5%, and cucumber seed powder 2%-5%. The egg laying poultry are fed with the feed additive and basal feed by the ratio of 1:10-1:20. Through the transformation of the feed additive in the egg laying poultry bodies, poultry eggs with low cholesterol and high HDL content (about 15 mg) are obtained. The poultry eggs eaten by people can increase the HDL level in human body by 80% and above, obviously relive the symptom of arteriosclerosis, and radically cure cardio-cerebrovascular disease after people eat the eggs for a long period. The feed additive has the advantages of high effective constituents and rich functional constituents. The materials in the feed additive are natural plants which grow widely, are easy to grow, get and free of toxins, can be eaten by people, fed to the poultry and used as medicine, and is suitable for the development and application of the poultry eggs with high nutritional value and health protection function.
Owner:王敏 +1

Preparing method for pig thrombin freeze-dried powder

The invention discloses a preparing method for pig thrombin freeze-dried powder. The preparing method comprises the following steps that anticoagulant pig plasma and gel are mixed and stirred for adsorption and pass through a column for elution, and a prothrombin solution is obtained; normal saline is added to rabbit brain powder, then the prothrombin solution and CaCl2 are added for zymogen activation, a crude thrombin enzyme solution is obtained, subjected to ultrafiltration for desalination and concentrated, viral inactivation is carried out, an obtained crude enzyme solution passes through DEAE-Sepharose Fast Flow chromatographic column, elution is carried out, target peaks are collected, and pig thrombin is obtained; the pig thrombin is added with mannitol or dextran 40, filtering, sterilizing, subpackaging, freeze drying and vacuum tamponing are carried out, an aluminum plastic combined cover is rolled, and a pig thrombin freeze-dried product is obtained; the freeze-dried product is subjected to dry heat treatment at 100 DEG C for secondary virus inactivation, and the pig thrombin freeze-dried powder is obtained after packaging. The specific activity of pig thrombin in the product is not lower than 130 U / mg, the whole process is simple in step and easy to implement, the product safety is improved, and the preparing method is suitable for industrial production.
Owner:WUHAN HITECK BIOLOGICAL PHARMA

Thromboelastography heparin quantitative detection kit and preparation method thereof

The invention relates to a thromboelastography heparin quantitative detection kit, which comprises a buffer agent, a blood coagulation factor Xa, rabbit brain congealed fat, a coagulation factor activator, a supporting agent, and a biological preservative. The preparation method comprises the following steps: preparing a buffer solution, a blood coagulation factor Xa stock solution, a blood coagulation factor activator stock solution, a biological preservative solution, and a rabbit brain congealed fat stock solution; taking the support agent and adding the buffer solution to prepare a supportsolution; adding the blood coagulation factor Xa, the blood coagulation factor activator, and the rabbit brain congealed fat stock solution to the supporting solution according to the requirements ofkit specification, adding the biological preservative solution after uniformly mixing, then adding the buffer solution to the specified amount, subpackaging and lyophilizing after uniformly mixing. The thromboelastography heparin quantitative detection kit provided by the invention can quantitatively detect the heparin in a sample by a thromboelastography, has good correlation in a linear range,meets the heparin detection limit standard and has a coefficient of variation of not more than 10%, and the sample adopts whole blood without extra treatment; the integrity of protein in a clotting cascade is also not required, and the inspection operating process is simplified, thereby facilitating doctors and patients.
Owner:上海原科实业发展有限公司

Activated partial thromboplastin time detection reagent and activated partial thromboplastin time detection method

The invention belongs to a clinical medicine detection technology, and particularly relates to an activated partial thromboplastin time detection reagent and an activated partial thromboplastin time detection method, wherein the detection reagent comprises a fresh rabbit brain impregnation liquid. According to the present invention, the method has advantages of precise detection and simple operation; and the safe, reliable and good-repeatability in vitro diagnostic reagent is provided for the endogenous blood coagulation factor deficiency and heparin therapy in clinical medicine.
Owner:北京众驰伟业科技发展有限公司

Prothrombin time assay kit and preparation method thereof

ActiveCN105368916ASolve the problem of uncontrolled sensitivityImprove accuracyMicrobiological testing/measurementBiological testingTissue factorProthrombin time assay
The invention discloses a prothrombin time assay kit and a preparation method thereof. The prothrombin time assay kit, which combines a buffer liquid system which contains a plurality of active ingredients with rabbit brain powder and a tissue factor ester, solves the problem that a single-ingredient reagent is incontrollable in sensitivity; and subsequently, a prothrombin time assay reagent, which is high in accuracy, strong in repeatability and good in stability, and is applicable to various semiautomatic / full-automatic coagulometers, is obtained.
Owner:WUHAN KING DIAGNOSTIC TECH CO LTD

Extraction buffer solution, rabbit brain extraction solution, PT detection reagent and PT detection kit

The invention relates to the field of medical detection, in particular to an extraction buffer solution, a rabbit brain extraction solution, a PT detection reagent and a PT detection kit. The extraction buffer solution comprises citrate or phosphate, anhydrous sodium acetate and water. With adding of the electrolyte, the repulsive force of charges between phospholipids is increased, so that the PTreagent is not easy to precipitate. The stability is enhanced; and the repeatability during testing is improved.
Owner:BEIJING SICCEEDER TECH CO LTD

Fibrinogen detection reagent/freeze-dried detection reagent for completely inhibiting function of platelets and preparation method of fibrinogen detection reagent/ freeze-dried detection reagent

PendingCN109932512AThe experimental results are accurate and stableReduce usageBiological testingFiberFreeze-drying
The invention relates to a fibrinogen detection reagent / freeze-dried detection reagent for completely inhibiting the function of platelets and a preparation method of the fibrinogen detection reagent / freeze-dried detection reagent. The detection reagent comprises a buffer solution, a supporting agent, rabbit brain congealed fat, a tissue factor, a platelet inhibitor, a platelet inhibiting enhancer, an organic solvent and a biological preservative; the freeze-dried detection reagent is a quantitative bottled freeze-dried product of the above detection reagent. According to the preparation method of the detection reagent, a buffer solution, a supporting liquid, a rabbit brain congealed fat liquid, a tissue factor liquid, a platelet inhibiting liquid, a platelet inhibiting enhancing liquid and the like are prepared; the liquids are mixed, and a biological preservative is added into an obtained mixture; and the supporting liquid is added to a newly obtained mixture in a full-dose manner. According to the preparation method of the freeze-dried detection reagent, the detection reagent is quantitatively bottled and frozen to be dried. According to the detection reagent / freeze-dried detection reagent provided by the invention, a thrombelastogram detection method is adopted, the function of platelets can be completely inhibited with no additional fibrinogen activators required; the false positive result of fibrinogens can be avoided; the accuracy and stability of detection can be ensured; a process can be simplified; and reagents can be saved.
Owner:上海原科实业发展有限公司

Ellagic acid reagent and preparation method thereof as well as activated partial thromboplastin time (APTT) determination reagent and APTT kit

The invention provides an ellagic acid reagent and a preparation method thereof as well as an activated partial thromboplastin time (APTT) determination reagent and an APTT kit and relates to the field of clinical diagnosis reagents. The preparation method comprises the following steps: adding ellagic acid into calcium-free purified water and rapidly stirring to uniformly disperse the ellagic acid; adding an alkaline buffering solution or inorganic alkali; rapidly adding an acidic buffering solution or organic acid and inorganic acid within 10min after the ellagic acid is added; adding metal ions; adding amino acid and a derivative thereof to obtain a buffering solution; furthermore, adding the calcium-free purified water into rabbit brain phospholipid and uniformly mixing and emulsifyingto obtain emulsified phospholipid; adding the emulsified phospholipid into the buffering solution and rapidly stirring and uniformly mixing to obtain the ellagic acid reagent. The technology is simpleand rapid and has detailed descriptions. The activated partial thromboplastin time determination reagent comprises the ellagic acid reagent and a calcium chloride reagent and has good stability. TheAPTT kit containing the activated partial thromboplastin time determination reagent can be used for directly replacing an imported high-stability APTT kit.
Owner:WUHAN CHANGLI BIOLOGICAL TECH CO LTD

In-vitro diagnostic kit for measuring prothrombin time

The invention discloses an in-vitro diagnostic kit for measuring prothrombin time. The in-vitro diagnostic kit comprises a prothrombin time measuring reagent and a plastic bottle for containing the prothrombin time measuring reagent, wherein the prothrombin time determination reagent is composed of a buffer solution system and thromboplastin, and the thromboplastin is obtained by taking rabbit brain powder as a raw material through extraction; the buffer solution system is prepared from the following raw materials: a buffer agent, a calcium ion reagent, a surfactant, amino acid, trehalose andprocline 300. In the kit disclosed in the present invention, the buffer solution system is creatively prepared by compounding the buffer agent, the calcium ion reagent, the surfactant, the amino acid,the trehalose and the proclin 300; through mutual cooperation and synergy with thromboplastin, the stability of the prothrombin time determination reagent can be improved on the basis of ensuring theaccuracy and sensitivity of the prothrombin time determination reagent.
Owner:SHENZHEN GOLDSITE DIAGNOSTICS

Processing method for industrially producing rabbit brain powder

The invention discloses a processing method for industrially producing rabbit brain powder. The method is characterized by comprising the following processes of: taking fresh rabbit brain, soaking the rabbit brain into cold acetone, fishing out the rabbit brain, removing blood vessels and meninges, adding the treated rabbit brain into the cold acetone, mixing the rabbit brain and the cold acetoneuniformly by using a homogenizer, performing centrifugation to remove the acetone solvent, and drying the rabbit brain powder. The method has the advantages that: because the traditional mortar for grinding is substituted by using the homogenizer, the activity of tissue factors in the rabbit brain is kept; the taken fresh rabbit brain is directly soaked into the cold acetone to substitute the traditional brine washing, so that the velocity of removing the blood vessels and the meninges in the rabbit brain is improved and the activity of the tissue factors is improved; the velocity of gas jet impact drying for rabbit brain powder protection with gas is improved by 2 to 3 times compared with the velocity of the traditional vacuum drying, and the rabbit brain powder is thinner, higher in activity and purer in color; and the whole method is high in production efficiency, and can realize industrialized large-scale production.
Owner:NINGBO UNIV

Cranial nerves rehabilitation medicine and its preparation method

Disclosed is a cranial nerves rehabilitation medicine and its preparation method, wherein the medicament is prepared from the following raw materials (by weight portion), rabbit brain 100-200, lichen 100-200, white fungus 50-70, buthus martensi kirsch 100-200, silkworm 80-150, earthworm 80-150, rhizoma Gastrodiae 80-150, Chinese angelica root 50-100, rhizome of Sichuan lovage 100-200, Sichuan aconite root 50-100, lubei 80-150, tabasheer 100-200, southern star 100-200, draconic dentes 80-150, amber 80-150, polygala root 80-150, calamus 50-80, Chinese data seeds 100-200.
Owner:宋维生

Prothrombin time test kit and preparation method thereof

A prothrombin time test kit consists of thromboplastin and a buffer liquid system, wherein the thromboplastin is rabbit brain tissue factors and recombinant tissue factors. The buffer liquid system comprises 30-50mM Tris-HCL, 3-10% of glycine, 1-5% of bovine serum albumin, 0.6-1.3% of sodium chloride, 6.8-8.4mM of calcium chloride and 30.5% of NaN, and the pH value of the buffer liquid system is 6.0-8.0. The thromboplastin also comprises rabbit cephalin. According to the invention, the defects that the sensitiveness indexes of various instruments are different due to the differences of the methods of the different instruments can be overcome, the high-sensitivity human recombinant thromboplastin and low-sensitivity rabbit brain powder extracting thromboplastin are combined, the PT reagent capable of meeting different methods of coagulometer can be prepared according to certain proportion, and the ISI (insulin sensitivity index) value is close to 1.0. The invention also discloses a preparation method of the prothrombin time test kit simultaneously.
Owner:武汉塞力斯生物技术有限公司

Feed additive for promoting growth

The invention discloses a feed additive for promoting growth. The additive is prepared from 11 parts of soybean protein active peptide powder, 10 parts of allium mongolicum regel powder, 5 parts of sunflower seed powder, 10 parts of flaxseed powder, 8 parts of rabbit brain powder, 9 parts of black sesame powder, 12 parts of brown sugar, 3 parts of endothelium corneum gigeriae galli powder, 11 parts of potassium iodide, 3 parts of sodium selenite, 2 parts of swallow bone powder and 3 parts of pomegranate peel. Thus, rich nutrients are provided, the additive can be easily absorbed by poultry by being added into feed, the feed absorption rate is increased, and palatability of the feed is improved.
Owner:黄健

Preparation method of thrombin

The present invention provides a preparation method of thrombin. The preparation method comprises that a prothrombin activator is added to a prothrombin-containing solution to activate prothrombin soas to obtain a thrombin-containing solution, and the prothrombin activator is selected from a recombinant lipidated tissue factor or a recombinant lipidated tissue factor and calcium ions. The methodfurther includes preparing the prothrombin-containing solution before activating prothrombin. The method further comprises the step of purifying and further treating the thrombin-containing solution to obtain a thrombin finished product. According to the preparation method disclosed by the invention, the recombinant lipidated tissue factor is used as an activator, so that compared with rabbit brain powder, the safety of a thrombin product can be remarkably improved, and the production cost is reduced; compared with soybean phospholipid and egg yolk phospholipid, the thrombin specific activityis obviously improved, and the method is very suitable for modern large-scale industrial production.
Owner:长春雷允上药业有限公司

A kind of production and processing method of rabbit brain powder

The invention relates to a production and processing method of rabbit brain powder. A production and processing method of rabbit brain powder, comprising the following steps: (1), soaking fresh rabbit brain in low-temperature acetone or saline to remove blood vessels and meninges; (2), removing the blood vessels and meninges of rabbit brains into Extrusion device soaked in acetone, squeeze the rabbit brain in the extrusion device into the grinder; (3), the grinder grinds the rabbit brain at a slow speed; (4), after grinding, start the filter at the bottom of the grinder , to further filter out blood vessels and meningeal impurities, then add acetone, shake a few times and then centrifuge, remove the acetone solvent after centrifugation, dry, subpackage, and store in a refrigerator at 4°C. The production and processing method of rabbit brain powder of the present invention further removes remaining more than 70% blood vessels and meningeal impurities through two steps of extruding and filtering; before grinding and centrifuging, add 20% acetone to reduce the colloidal state of the solution. It reduces the difficulty of subsequent centrifugation and drying while maintaining the activity of the product.
Owner:青岛康大爱博生物科技有限公司

Buffer composition for purifying tissue factor, purification preparation, PT detection composition and PT detection kit

The invention relates to the field of detection, in particular to a buffer composition for purifying a tissue factor, a purification preparation, a PT (prothrombin time) detection composition and a PTdetection kit. A key raw material, namely tissue thromboplastin, is prepared by a genetic engineering mode; high-purity r-TF (recombinant tissue factor) can be obtained on a large scale by a fermentation technology and a purification technology, and the problems that tissues such as rabbit brains and placentas are difficult in source, big in difference between batches and low in sensitivity are solved. A high-sensitivity prothrombin PT diagnosis kit based on r-TF liquid type has high stability, small difference between batches and high sensitivity, is mainly applied to screening of a clinicalextrinsic coagulation pathway, monitoring of oral warfarin medicines and auxiliary diagnosis of diseases such as liver disease, and can be traced back to an international standard product PT reagent,so that detection comparability of reagents among different reference laboratories and different manufacturers is achieved.
Owner:BEIJING SICCEEDER TECH CO LTD

Ruminant staphylococcus separation, bacteria propagation and capsular polysaccharide expression culture medium

InactiveCN101063092ASave strongPassage virulence maintenance ability is strongBacteriaMicroorganism based processesDipotassium hydrogen phosphateVaccine Production
The invention discloses a separating, enriched and capsular polysaccharide expressing medium of ruminant staphylococcus, which comprises the following steps: choosing milky protein hydrolysate, protease leather, tryptone, soy peptone, lactin, common salt, dipotassium hydrogen phosphate, magnesium sulfate, ferrosi sulfas, L-cysteine hydrochlorate, rabbit brain heart drench and double distilled water as raw material; shearing fresh rabbit brain and heart; grinding; homogenizing; soaking with double distilled water under 4 deg. c; boiling for 15 min; filtering with filter paper; compensating water; getting the rabbit brain heart drench. This invention possesses strong ability of bacterial maintain and passage toxic force, which is fit for separating staphylococcus.
Owner:新疆维吾尔自治区畜牧科学院兽医研究所

Chinese medicine for tonifying kidney, invigorating heart and spleen, and strengthening function of human body and preparation method thereof

The invention relates to a traditional Chinese medicine for tonifying kidney, strengthening heart and spleen, and enhancing function of human body, and a preparation method thereof. The preparation method comprises the following steps: adding water into ten gouts of traditional Chinese medicine comprising prepared rhizome of rehmannia, angelica, sauted white paeony root, asparagus, dwarf lilyturf turber, sauted Atractylis ovata, desertliving cistanche, tuckahoe with pine, sauted spina date seed and honey-soaked milkwort, then decocting the mixture thrice, mixing the thrice decoction, condensing filtered decoction into extract, adding red ginseng, dog kidney, rabbit brain, amber, natural indigo, sharpleaf galangal fruit and grassleaf sweelflag rhizome into the extract, crushing and sieving the components respectively, then evenly mixing the fine powder, adding proper amount of starch into the fine powder to prepare granules, and filling the granules into hollow capsules to obtain the traditional Chinese medicine capsule. The traditional Chinese medicine not only has good curative effect on kidney essence deficiency and heart-spleen deficiency, and has the efficacies of replenishing qi to invigorate the spleen, enriching blood to nourish the heart, nourishing the kidney and replenishing essence, but also has the advantages of short treatment course by oral administration, quick effect, little toxic and side effects, and convenience for carrying, and simultaneously has the advantages of rich raw material sources, simple preparation method and low cost.
Owner:安徽张恒春药业股份有限公司

A prothrombin time assay kit and preparation method thereof

ActiveCN105368916BSolve the problem of uncontrolled sensitivityImprove accuracyMicrobiological testing/measurementBiological testingTissue factorProthrombin time assay
The invention discloses a prothrombin time assay kit and a preparation method thereof. The prothrombin time assay kit, which combines a buffer liquid system which contains a plurality of active ingredients with rabbit brain powder and a tissue factor ester, solves the problem that a single-ingredient reagent is incontrollable in sensitivity; and subsequently, a prothrombin time assay reagent, which is high in accuracy, strong in repeatability and good in stability, and is applicable to various semiautomatic / full-automatic coagulometers, is obtained.
Owner:WUHAN KING DIAGNOSTIC TECH CO LTD

A kind of ellagic acid reagent and its preparation method and activated partial thromboplastin time determination reagent, aptt kit

The invention provides an ellagic acid reagent and a preparation method thereof as well as an activated partial thromboplastin time (APTT) determination reagent and an APTT kit and relates to the field of clinical diagnosis reagents. The preparation method comprises the following steps: adding ellagic acid into calcium-free purified water and rapidly stirring to uniformly disperse the ellagic acid; adding an alkaline buffering solution or inorganic alkali; rapidly adding an acidic buffering solution or organic acid and inorganic acid within 10min after the ellagic acid is added; adding metal ions; adding amino acid and a derivative thereof to obtain a buffering solution; furthermore, adding the calcium-free purified water into rabbit brain phospholipid and uniformly mixing and emulsifyingto obtain emulsified phospholipid; adding the emulsified phospholipid into the buffering solution and rapidly stirring and uniformly mixing to obtain the ellagic acid reagent. The technology is simpleand rapid and has detailed descriptions. The activated partial thromboplastin time determination reagent comprises the ellagic acid reagent and a calcium chloride reagent and has good stability. TheAPTT kit containing the activated partial thromboplastin time determination reagent can be used for directly replacing an imported high-stability APTT kit.
Owner:WUHAN CHANGLI BIOLOGICAL TECH CO LTD

Polypeptide-factor cosmetic and preparation method thereof

The invention provides a polypeptide-factor cosmetic and a preparation method thereof. The polypeptide-factor cosmetic is prepared from the following raw materials in parts by weight: 0.2 to 0.6 part of carbomer 974, 0.5 to 3.5 parts of honey, 0.5 to 1.5 parts of a ginseng extract, 0.5 to 3.5 parts of a lecithin extract, 4-8 parts of a plant extract, 6-10 parts of a rabbit brain extract, 4 to 8 parts of xanthan gum, 0.5 to 1.5 parts of peregal, 0.5 to 3.5 parts of glycerol, 0.8 to 1.2 parts of octadecanol, 0.5 to 1.5 parts of hexadecanol, 0.5 to 1.5 parts of glyceryl stearate, 0.5 to 3.5 parts of ethylparaben, 2-6 parts of hyaluronic acid and 6-10 parts of sodium hydroxide. The polypeptide-factor cosmetic can be used for effectively decomposing and fading black spots and chromatosis, improving skin color, diminishing inflammation, removing acnes, resisting aging and preventing wrinkles; and the polypeptide-factor cosmetic can be used for resisting oxidation and protecting skin from being damaged by ultraviolet rays, is safe and non-toxic, is easily available in raw materials and is suitable for being industrially produced.
Owner:陈勇

Processing method for industrially producing rabbit brain powder

The invention discloses a processing method for industrially producing rabbit brain powder. The method is characterized by comprising the following processes of: taking fresh rabbit brain, soaking the rabbit brain into cold acetone, fishing out the rabbit brain, removing blood vessels and meninges, adding the treated rabbit brain into the cold acetone, mixing the rabbit brain and the cold acetoneuniformly by using a homogenizer, performing centrifugation to remove the acetone solvent, and drying the rabbit brain powder. The method has the advantages that: because the traditional mortar for grinding is substituted by using the homogenizer, the activity of tissue factors in the rabbit brain is kept; the taken fresh rabbit brain is directly soaked into the cold acetone to substitute the traditional brine washing, so that the velocity of removing the blood vessels and the meninges in the rabbit brain is improved and the activity of the tissue factors is improved; the velocity of gas jet impact drying for rabbit brain powder protection with gas is improved by 2 to 3 times compared with the velocity of the traditional vacuum drying, and the rabbit brain powder is thinner, higher in activity and purer in color; and the whole method is high in production efficiency, and can realize industrialized large-scale production.
Owner:NINGBO UNIV

Thromboelastometry heparin quantitative detection kit and preparation method thereof

ActiveCN108982865BQuantitative detection is convenient and accurateEasy to detectBiological material analysisBiological testingCoagulation Factor XaThrombus
A kit for quantitative detection of heparin by thromboelastography, comprising a buffer, blood coagulation factor Xa, rabbit brain fat coagulation, blood coagulation factor activator, support agent, biological preservative; the preparation method includes: preparing buffer solution, blood coagulation factor Xa stock solution, Blood coagulation factor activator stock solution, biological antiseptic solution, rabbit brain lipid coagulation stock solution; take support agent and add buffer solution to prepare support solution; add coagulation factor Xa, coagulation factor activator, rabbit brain fat coagulation stock solution according to kit specifications In the support solution, add biological preservative solution after mixing, and then add buffer solution to the specified amount, mix and freeze-dry. The invention can quantitatively detect the heparin in the sample by the thromboelastography detection method, the correlation is good in the linear range, meets the detection limit standard of heparin, and the coefficient of variation is not more than 10%. There is also no requirement for the integrity of the protein in the waterfall, which simplifies the inspection process and is convenient for doctors and patients.
Owner:上海原科实业发展有限公司

Egg-laying bird feedstuff additive

The invention relates to an egg laying poultry feed additive for supplying and adding a dietary factor. The constituents and the weight percentages thereof are as follows: soy protein bioactive peptides powder 25-30%, allium mongolicum powder 15-20%, sunflower seed powder 2%-5%, linseed 3%-5%, hemp seed powder 3%-5%, rabbit brain powder 5%-10%, perillaseed powder 5%-10%, black sesame seed powder 5%-10%, parslane herb powder 5%-10%, brown sugar 5%-10%, chicken's gizzard-membrane powder 2%-5%, dried orange peel powder 3%-5%, and cucumber seed powder 2%-5%. The egg laying poultry are fed with the feed additive and basal feed by the ratio of 1:10-1:20. Through the transformation of the feed additive in the egg laying poultry bodies, poultry eggs with low cholesterol and high HDL content (about 15 mg) are obtained. The poultry eggs eaten by people can increase the HDL level in human body by 80% and above, obviously relive the symptom of arteriosclerosis, and radically cure cardio-cerebrovascular disease after people eat the eggs for a long period. The feed additive has the advantages of high effective constituents and rich functional constituents. The materials in the feed additive arenatural plants which grow widely, are easy to grow, get and free of toxins, can be eaten by people, fed to the poultry and used as medicine, and is suitable for the development and application of thepoultry eggs with high nutritional value and health protection function.
Owner:王敏 +1

A kind of thromboplastin and its extraction method and pt reagent

The invention relates to the technical field of biochemical detection and discloses thromboplastin, an extraction method thereof and a PT reagent. According to the extraction method, a buffering solution low in metal chelating capacity and a non-ionic surface active agent are added into rabbit brain powder, and oscillating extraction is performed; and then centrifuging is performed, and obtained supernate is the thromboplastin. According to the extraction method, in the process of extracting the thromboplastin with the rabbit brain powder as raw materials, the specific buffering solution and the non-ionic surface active agent are selected for performing extraction, the extracted thromboplastin consumes short time, and the extraction amount is large; and when PT is detected, it is only needed to incubate to-be-detected blood plasma for 1 min, and compared with long incubation time of an existing PT reagent, the thromboplastin can improve the detection efficiency.
Owner:SINOCARE

Preparation method of freeze-dried rabbit brain tissue factor

The invention discloses a preparation method for a rabbit brain tissue factor freeze-drying preparation. The preparation method comprises the following steps: taking a fresh rabbit brain and stripping meninx and blood vessels; removing a brainstem and washing by using normal saline; putting the rabbit brain into a cleaning mortar and adding acetone until the rabbit brain is immersed; grinding by using a grinding hammer and pouring off the acetone; repeating for three times; filtering the acetone by using filtering paper; putting the rabbit brain into an oven of 37 DEG C and paving to evaporate and dry the acetone; adding the normal saline; uniformly agitating and putting a mixture into a constant-temperature water bath of 37 DEG C to be pre-heated and activated, incubated and agitated; centrifuging for separating; taking liquid supernatant and filtering to obtain a rabbit brain FIII tissue factor suspension solution; adding the rabbit brain FIII tissue factor suspension solution into a small bottle; freezing-drying, exhausting and pressing a bottle to prepare the rabbit brain tissue factor freeze-drying preparation, and storing at -20 DEG C. With the adoption of the scheme, the technology is very mature, the quality is very stable and the guarantee period is very long; the preparation method is very convenient to use; the preparation method has very high medical teaching, scientific research, clinical diagnosis and treatment and economic values.
Owner:WANNAN MEDICAL COLLEGE
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