| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 荷斯坦成年母牛繁育教学培训模型 | CN202120594836.4 | 2021-03-24 | CN214955604U | 2021-11-30 | 王建华; 李培培; 张宝珣 |
| 本实用新型涉及建立动物实验模型技术领域，具体涉及一种荷斯坦成年母牛繁育教学培训模型：包括标准设计尺寸的中空的母牛模型主体；母牛模型主体后部设有侧开门，母牛模型主体内部通过固定件连接安装有可拆卸的直肠、子宫及子宫附件；直肠贯通连接仿生的肛门，子宫贯通连接仿生的阴户；母牛模型主体后端设有仿生的尾部，尾部由软性材料制成。本实用新型建立了一种可用于荷斯坦牛育种教学、牛体况评分（BCS）、牛体型外貌评分、牛体尺测量、牛发情鉴定及人工输精操作模拟训练的动物模型，与真牛教学相比，采用模型教学可以不受牧场时间、场所和牛只选择及防疫等问题，而且会降低教学、培训成本，减少对牧场牛只的损伤和影响。 | ||||||
| 2 | 一种肉牛新品种的培育方法 | CN202311067745.5 | 2023-08-23 | CN117296787A | 2023-12-29 | 杜书增; 朱春梅; 杨红玉; 王剑; 张吉昌; 张蔚; 张云征; 曹杰; 王建钦 |
| 本发明公开了一种肉牛新品种的培育方法,以南阳牛为母本，以夏洛莱牛为父本，进行杂交生产得到夏南杂交一代牛群；然后用夏南杂交一代牛群中的母牛再与皮埃蒙特牛公牛进行杂交，得到皮夏南杂交二代牛群；然后再用皮夏南杂交二代牛群中的母牛与皮埃蒙特牛公牛进行级进杂交，得到皮夏南杂交三代牛群，选择皮夏南三代牛群中的优秀母牛和公牛进行横交固定、自群繁育，最终得到皮夏南新品种。本发明培育的皮夏南新品种被毛主要为灰白色和灰黑色，成年公牛体重850～960千克，成年母牛体重550～670千克，一个周期泌乳量在1850～2790千克。此新品种具有出肉率高、肉质好的优点，净肉率比南阳牛高7.6％，胆固醇比南阳牛低32％，脂肪含量比南阳牛低27％。 | ||||||
| 3 | 来曲唑在用于制备成年牛超数排卵药物中的应用 | CN201110436200.8 | 2011-12-22 | CN103169699B | 2014-11-12 | 田见晖; 贾振伟; 吴中红; 张家新; 安磊 |
| 本发明提供了一种来曲唑在用于制备成年牛超数排卵药物中的应用。本发明在传统成年母牛超排方案中增加使用LE，利用来曲唑对内分泌及旁分泌的影响及卵巢卵泡募集的作用，促进卵泡的发育，增加可利用的卵母细胞数量；另外其半衰期较短，代谢速度快，无副作用，能够成为家畜超排辅助药物在畜牧业生产上推广应用。 | ||||||
| 4 | 来曲唑在用于制备成年牛超数排卵药物中的应用 | CN201110436200.8 | 2011-12-22 | CN103169699A | 2013-06-26 | 田见晖; 贾振伟; 吴中红; 张家新; 安磊 |
| 本发明提供了一种来曲唑在用于制备成年牛超数排卵药物中的应用。本发明在传统成年母牛超排方案中增加使用LE，利用来曲唑对内分泌及旁分泌的影响及卵巢卵泡募集的作用，促进卵泡的发育，增加可利用的卵母细胞数量；另外其半衰期较短，代谢速度快，无副作用，能够成为家畜超排辅助药物在畜牧业生产上推广应用。 | ||||||
| 5 | 基于人工智能及航拍图像的牧区母牛护犊行为检测方法 | CN202010668639.2 | 2020-07-13 | CN111814698A | 2020-10-23 | 贾靖雯; 洪子俊 |
| 本发明公开了一种基于人工智能及航拍图像的牧区母牛护犊行为检测方法。包括：对牧区航拍图像进行分析生成牛关键点热力图、关键点的关联矢量场；应用条件约束的匹配算法，通过最大权重匹配获得最终匹配关系，为每个头部关键点匹配一个尾部关键点；计算所有相匹配的两个关键点坐标距离，判断对象是成年牛还是牛犊；计算每两只牛之间的距离，若判断结果为过于靠近分析两只牛的尺寸及血缘关系判断是否存在母牛护犊行为；进行图像拼接结合WebGIS技术对牧区建筑信息模型进行可视化。利用本发明，能对牧区整体散养情况进行监督并检测散养期间的母牛护犊行为。 | ||||||
| 6 | 夏南牛与德国黄牛杂交养殖方法 | CN201410615637.1 | 2014-11-05 | CN104509492A | 2015-04-15 | 陈仁杰; 郭群 |
| 本发明涉及一种夏南牛与德国黄牛杂交养殖方法，本发明培育得到的夏南牛与德国黄牛杂交新品种具有以下的特点：体质健壮，性情温驯，适应性强，遗传性能稳定，生长周期短；具有较高的优质牛肉率、屠宰率、净肉率和产奶量，增重快，成年公牛体重达1000kg以上，母牛体重达700kg以上，而且还具有良好耐热性，耐寒冷和抗病性。 | ||||||
| 7 | 畜用安情助长注射液 | CN99112975.X | 1999-06-01 | CN1277023A | 2000-12-20 | 初冬雪 |
| 一种畜用安情助长注射液,根据医药原理,以蛋氨酸、肌苷、醋酸甲羟孕酮为原料,用蒸馏水稀释而成。适于成年母猪、母羊、母牛等,使家畜避免发情并促其快速生长。经百余例的应用验证,药效显著,家畜平均日增重1—2斤,有效率98%以上,成活率100%。原料属药品,无任何毒副作用,对人畜无害。药源丰富,用量少,价格低廉,制作简单,使用方便。避免了家畜因阉割创伤,影响生长以至生病死亡,可提高养殖业的经济效益。 | ||||||
| 8 | 一种肉牛幼牛期的饲养方法 | CN201710054997.2 | 2017-01-24 | CN106857395A | 2017-06-20 | 谭春萍; 张艳雯; 黄广君; 黄福标; 于冬玲; 蒙超; 胡玉平 |
| 本发明涉及禽畜养殖技术领域，尤其涉及一种肉牛幼牛期的饲养方法，具体为：出生后采食母乳5‑7d后，与母牛分开饲喂，犊牛转入设置有发酵床的牛舍进行饲养，每日饲喂代乳料，每天喂食3次，代乳料组成为：苜蓿草40‑70重量份、车轴草20‑50重量份、玉米青贮80‑100重量份、榕树须提取物10‑18重量份、南瓜藤提取物25‑45重量份、腐胺1‑4重量份、酵母细胞壁多糖3‑7重量份、燕窝唾液酸糖蛋白0.5‑1.3重量份；于30日龄时，添加成年牛精饲料，并限制每日每头的精饲料采食量为0.3‑0.6kg；该法能有效地促进消化吸收，并起到抗病防病的效果。 | ||||||
| 9 | 一种利用发酵床对幼牛进行饲养的方法 | CN201611246792.6 | 2016-12-29 | CN106719420A | 2017-05-31 | 杨远澄; 周贵金; 谭春萍; 杨远广; 陆海龙; 欧庆卫; 李政 |
| 本发明涉及禽畜养殖技术领域，尤其涉及一种利用发酵床对幼牛进行饲养的方法，具体为：出生后采食母乳5‑7d后，与母牛分开饲喂，犊牛转入设置有发酵床的牛舍进行饲养，发酵床中设置有发酵垫料，每日饲喂代乳料，每天喂食3次，代乳料组成为：苜蓿草40‑70重量份、车轴草20‑50重量份、玉米80‑100重量份、山楂10‑30重量份、紫菜17‑35重量份、白萝卜10‑30重量份、腐胺1‑4重量份、酵母细胞壁多糖3‑7重量份、燕窝唾液酸糖蛋白0.5‑1.3重量份；于45日龄时，添加成年牛精饲料，并限制每日每头的精饲料采食量为0.3‑0.6kg；该法操作简单易行，能有效地促进消化吸收，并起到抗病防病的效果。 | ||||||
| 10 | 一种牛基本信息记录装置 | CN202320724562.5 | 2023-04-04 | CN219214526U | 2023-06-20 | 杨建春; 王鸿盛; 伏中方; 刘永勤; 汪楠 |
| 本实用新型涉及牧兽信息记录领域，公开了一种牛基本信息记录装置，包括盖板，所述盖板一侧铰接设置有连接机构，所述连接机构一侧固定设置有主体机构，所述主体机构后端上侧固定设置有扫描机构。本实用新型中，盖板用于将主体机构覆盖，第一记录本用于记录成年的母牛，第二记录本用于记录成年的公牛，第三记录本用于记录体重未达到成年标准的娟珊牛，将不同性别和重量的娟珊牛数据进行分类记录，用于保护记录的数据信息，连接机构起到连接盖板和主体机构的同时内部也放置有书写笔，便于使用，扫描机构用于扫描娟珊牛的耳标，将其名称和其记录的基本信息进行核实记录，用于确定每一个娟珊牛的信息名称，保证信息记录的准确性。 | ||||||
| 11 | 一种用于放牧的新型犊牛舍 | CN201720867029.9 | 2017-07-17 | CN206978351U | 2018-02-09 | 刘洪瑜; 庄静仪; 兰延坤; 王歆; 朱小云; 尚慧; 王家国; 童莉; 李福宝; 夏宣保; 林燕 |
| 本实用新型涉及畜禽养殖技术领域，具体涉及一种用于放牧业的新型犊牛舍，包括立柱及立柱之间的围栏单元围设出的犊牛舍，立柱的上方盖设有顶棚，所述的犊牛舍内布置有若干穹顶式犊牛岛、还包括有饲槽和水桶供补饲犊牛，所述的围栏单元包括竖杆及横杆构成的框架，且至少一侧的围栏单元上的竖杆沿横杆限位移动供控制犊牛舍进出口开度；所述的围栏单元可控制犊牛进出口开度，避免成年母牛进入犊牛舍内，从而对犊牛进行针对性的补饲，或提供特殊的饲料确保犊牛的迅速增重，提高犊牛存活率的同时控制了饲养成本。 | ||||||
| 12 | Dietetical slide rule | JP5428579 | 1979-05-02 | JPS55146567A | 1980-11-14 | SANADA HIROMICHI |
| PURPOSE: To easily calculate by use of an exclusive slide rule as to feed for animals based upon total amount of digestible nutrition (TDN) and amount of digestible raw protein (DCP), which are considered to be the most important for a breeding control. CONSTITUTION: A necessary nutrition amount which is requred for rearing a cow shows a curve to its weight, and a nutrition amount required for keeping a grown- up cow can be linearized. For instance, as for the nutrition amount required for rearing a cow, a horizontal axis, a vertical axis and a straight line extending at an angle of 45° from the origin show DCP amount, TDN amount and weight, respectively. A curve above the afore-mentioned oblique line shows TDN amount to be derived of a calf which is growing, and a curve above the former shows TDN amount of a grown-up cow which is in the final two or three months of pregnancy. A curve on the right of the oblique line shows DCP amount to be derived in the same way, and furthermore a curve on the right of the former shows DCP amount to be derived concerning a cow which is pregnant. B is that which has added the nutrition amount of a grown-up cow to A, and becomes a fixed plate. C is a plan of a slide rule. COPYRIGHT: (C)1980,JPO&Japio | ||||||
| 13 | Method and product for treating failure of passive transfer and improving milk production in bovine species | US239886 | 1994-05-09 | US5645834A | 1997-07-08 | Richard H. Cockrum |
| A product and method of treating failure of passive immunity transfer and for stimulating growth and milk production in cows by administration of proteins purified from bovine colostrum is disclosed. Injecting, either subcutaneously or intravenously, prepared bovine colostrum containing immunoglobulins and nonspecific proteins increases immunoglobulins in the blood stream to effect passive transfer after gut closure. Also administration in spray dried form as a diet supplement to growing calves or adult cows improves growth and milk production due to the presence of previously unappreciated nonspecific proteins. | ||||||
| 14 | INCREASING THE STABILITY OF RECOMBINANT ADULT HUMAN APOHEMOGLOBIN | PCT/US2005032627 | 2005-09-15 | WO2006031840A3 | 2006-05-11 | OLSON JOHN S; PHILLIPS GEORGE N JR |
| The disclosure relates to recombinant adult human apohemoglobin (apo-rHb) in which the stability has been increased by replacement of an amino acid with a counterpart from another organsim, such as a deep sea diving mammal. This mutated apo-rHb may be more stable and/or give higher production yields than unmutated adult human apo-rHb. The mutated apo-rHb may be produced in microorganisms, such as E. coli or yeast cells, or animal erythroid cells. Some apo-rHb of the present disclosure may be used as part of a blood substitute. | ||||||
| 15 | External development of bovine egg fertilized in vitro | JP27990989 | 1989-10-30 | JPH02227016A | 1990-09-10 | NAKAO HARUHIKO; NAKATSUJI NORIO |
| PURPOSE: To improve the development efficiency of fertilized egg during the period to return into the uterus of an adult cow by maturing and fertilizing a bovine egg in vitro and co-culturing the fertilized egg together with a trophoblast vesicle of bovine, thereby developing the bovine cell fertilized in vitro. CONSTITUTION: External development of a bovine egg fertilized in vitro is carried out by maturing and fertilizing a bovine egg in vitro and co-culturing the fertilized egg together with a trophoblast vesicle of bovine, thereby developing the bovine cell fertilized in vitro. As an alternative method, a fertilized bovine egg matured and fertilized in vitro is co-cultured together with a bovine trophoblast vesicle or bovine cumulus cell in a medium added with EDTA to develop the egg to a stage transplantable to the uterus of cow. The co-culture of the fertilized bovine egg is carried out in a medium having a bovine fetus serum concentration of 1-5%, to which EDTA is added and free from caloric source while keeping the oxygen concentration in the gaseous phase to 2-10%. COPYRIGHT: (C)1990,JPO&Japio | ||||||
| 16 | Increasing the stability of recombinant adult human apohemoglobin | US11724007 | 2007-03-14 | US07803912B2 | 2010-09-28 | John S. Olson; George N. Phillips, Jr. |
| The disclosure relates to recombinant adult human apohemoglobin (apo-rHb) in which the stability has been increased by replacement of an amino acid with a counterpart from another organism, such as a deep sea diving mammal. This mutated apo-rHb may be more stable and/or give higher production yields than unmutated adult human apo-rHb. The mutated apo-rHb may be produced in microorganisms, such as E. coli or yeast cells, or animal erythroid cells. Some apo-rHb of the present disclosure may be used as part of a blood substitute. | ||||||
| 17 | Increasing the stability of recombinant adult human apohemoglobin | US11724007 | 2007-03-14 | US20070172924A1 | 2007-07-26 | John Olson; George Phillips |
| The disclosure relates to recombinant adult human apohemoglobin (apo-rHb) in which the stability has been increased by replacement of an amino acid with a counterpart from another organism, such as a deep sea diving mammal. This mutated apo-rHb may be more stable and/or give higher production yields than unmutated adult human apo-rHb. The mutated apo-rHb may be produced in microorganisms, such as E. coli or yeast cells, or animal erythroid cells. Some apo-rHb of the present disclosure may be used as part of a blood substitute. | ||||||
| 18 | TRANSGENIC CLONED COW PRODUCING HUMAN PROUROKINASE AND METHOD FOR PRODUCING THE SAME | PCT/KR2003/001657 | 2003-08-16 | WO2004016773A1 | 2004-02-26 | HWANG, Woo-Suk; LEE, Byeong-Chun; KANG, Sung-Keun; JEUNG, Eui-Bae; CHO, Jong-Ki; MMU, Bhuiyan; KIM, Soon-Woong; PARK, Eul-Soon; JANG, Goo; PARK, Jung-Su; KIM, Sung-Ki |
Disclosed is a method of producing a transgenic cloned cow expressing human prourokinase by gene targeting using a transfection technique in combination with somatic cell cloning, comprising the steps of introducing an exogenous gene encoding human prourokinase into adult cow-derived somatic cells and producing a cloned cow using the transfected somatic cells carrying the exogenous gene expressing human prourokinase, and a transgenic cloned cow produced by such a method. Also, the present invention discloses a method of obtaining human prourokinase from cow’s milk using such a transgenic cloned cow expressing human prourokinase in the mammary gland. |
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| 19 | 사람 에리트로포이에틴을 생산하는 형질전환 복제소 및이의 생산 방법 | KR1020030033582 | 2003-05-27 | KR1020040101793A | 2004-12-03 | 황우석; 이병천; 강성근; 정의배; 조종기; 김순웅; 박을순; 장구; 박희정 |
| PURPOSE: Transgenic cloned cow producing human erythropoietin and a method for producing the same transgenic cloned cow are provided, which method allows economic and effective production of various biomedicines, and facilitates production of human erythropoietin in cow's milk. CONSTITUTION: The nuclear transfer embryo produced by a fusion of a cow-derived enucleated oocyte with a nucleus of a cow-derived somatic cell transfected with a gene encoding human erythropoietin is provided, wherein the cow is an adult; the nuclear transfer embryo is SNU-B4(KCTC 10450BP). The method for producing a transgenic cloned cow expressing human erythropoietin in the mammary gland comprises the steps of: (a) introducing a gene encoding human erythropoietin into a cow-derived somatic cell line to prepare a nuclear donor cell; (b) removing cumulus cells surrounding a recipient oocyte and then the cytoplasm including the first polar body from the oocyte to prepare a cow-derived enucleated recipient oocyte; (c) transferring the transfected nuclear donor cell into the enucleated recipient oocyte and carrying out cell fusion to generate nuclear transfer embryos; and (d) transplanting the nuclear transfer embryo into a surrogate mother cow to produce live offspring. | ||||||
| 20 | Ectosomatic generation of bovine embryo | JP16546792 | 1992-06-02 | JPH06197666A | 1994-07-19 | SATO TAKESHI; KOBAYASHI KEIZO; HOSHI HIROYOSHI; OIKAWA TANEAKI |
| PURPOSE: To enable the ectosomatic generation of bovine embryo without causing troubles such as scattering of the embryogenetic results by the lot of serum and infection with virus, etc., by culturing a fertilized bovine ovum in vitro in a serum-free medium in the presence of a metalloproteinase inhibitor. CONSTITUTION: Ovary of an adult cow collected within 3 hr after slaughter is put into a plastic bag, transported in a state warmed with water of 30-34°C, cut into two with surgical scissors and finely incised with a surgical knife. Ovum attached with granulosa cells is collected, washed, put into a maturation medium and subjected to maturation culture at 38.5°C for 20-22hr in an incubator containing humidified atmosphere having carbon dioxide gas concentration of 5%. Separately, frozen semen of a Japanese Black Cattle is melted in warm water of 35°C, mixed with the ovum, fertilized by culturing at 38.5°C for 6 hr in an incubator containing humidified atmosphere having carbon dioxide gas concentration of 5% and the fertilized bovine ovum is cultured in vitro in a serum-free medium in the presence of a metalloproteinase inhibitor to achieve the ectosomatic generation of bovine embryo without causing the troubles such as scattering of the embryogenetic results and the infection with virus, etc. COPYRIGHT: (C)1994,JPO&Japio | ||||||
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