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    • 1. 发明授权
    • 채혈백 보관함
    • BLOOD GATHERING BAG存款箱
    • KR100754743B1
    • 2007-09-03
    • KR1020060065542
    • 2006-07-12
    • 세원셀론텍(주)
    • 이근성장동일이준근임소혁서동삼장정호
    • A61J1/05A61J1/00
    • A61J1/05B65D25/10B65D2571/00333
    • A blood gathering bag depository case is provided to perform a more efficient process work after gathering cord blood and to keep the blood gathering bags more safely, thereby improving a quality and reliability of a product. A blood gathering bag depository case includes a rectangular case body(11) formed long in a longitudinal direction, and having a front plate(12), a rear plate(13), and plural partitions(14) formed therein at regular intervals so as to store plural blood gathering bags separately. The partitions are formed to be inclined so as to be useful to insert and take out the blood gathering bag, and separate blood plasma from the blood easily by a tilt.
    • 提供采血袋存放箱,在收集脐带血后进行更有效的处理工作,并使血液收集袋更安全,从而提高产品的质量和可靠性。 集血袋存放箱包括长度方向形成的矩形盒体(11),并且具有前板(12),后板(13)和以规定间隔形成的多个隔板(14),以便 分开储存多个采血袋。 分隔壁形成为倾斜的,以便插入和取出血液收集袋,并且通过倾斜容易地将血浆与血液分离。
    • 5. 发明授权
    • 연골조직 수복용 조성물의 제조방법
    • 制剂组织修复组合物的制造方法
    • KR101279812B1
    • 2013-06-28
    • KR1020120052141
    • 2012-05-16
    • 세원셀론텍(주)
    • 여세근장정호유지철서동삼이준근우상훈
    • A61L27/24A61L27/20A61F2/30
    • A61K38/39A61K31/728A61L27/26A61L2400/06A61L2430/06A61M5/31A61M2210/02C08L5/08C08L89/06
    • PURPOSE: A manufacturing method of compositions for repairing cartilage tissue is provided to easily and rapidly induce cartilage repair and regeneration by removing a burden related to animals, excluding humans. CONSTITUTION: A manufacturing method of compositions for repairing cartilage tissue comprises the following steps: manufacturing collagen in which a diluted concentration is 5-60 mg/mL except for water which melts the collagen or a physiological buffer solution; manufacturing phosphorus hyaluronic acid in which a diluted concentration of 5-20 mg/mL except for water which melts the collagen or a physiological buffer solution; intermixing the collagen and hyaluronic acid by using a bidirectional scanner or a mixer; and removing bubbles using a centrifuge and centrifuging at 2000-5000 G. The centrifuge maintains room temperature at 1-30 deg. Celsius.
    • 目的:提供用于修复软骨组织的组合物的制造方法,通过去除与人类不同的动物相关的负担来容易且快速地诱导软骨修复和再生。 构成:用于修复软骨组织的组合物的制造方法包括以下步骤:制造其中稀释浓度为5-60mg / mL的胶原,除了熔化胶原蛋白或生理缓冲溶液的水; 制造除了熔化胶原蛋白或生理缓冲溶液的水以外的5-20mg / mL的稀释浓度的磷透明质酸; 使用双向扫描仪或混合器混合胶原蛋白和透明质酸; 并使用离心机除去气泡并在2000-5000 G离心。离心机保持室温在1-30度。 摄氏度。
    • 6. 发明授权
    • 중간엽 줄기세포 기본 배양 배지 조성방법, 중간엽 줄기세포 기본 배양 배지 및 이를 이용하여 배양분화된 세포치료제
    • 用于制造基质培养基的方法,用于骨髓干细胞的基础培养基,用于培养和分化的细胞干细胞和细胞培养基的培养基
    • KR101138091B1
    • 2012-04-24
    • KR1020110087498
    • 2011-08-31
    • 세원셀론텍(주)
    • 서동삼이준근장동일최민정김장훈김가람장정호
    • C12N5/0775C12N1/38
    • C12N5/0667C12N5/0663C12N2500/32C12N2500/34C12N2500/38C12N1/38
    • PURPOSE: A basic culture medium for mesenchymal stem cells is provided to enhance stem cell proliferation rate and to shorten culture time. CONSTITUTION: A basic culture medium for mesenchymal stem cells, ABM-M(advanced basic media-mesenchymal stem cell), has basic DMEM high glucose medium and contains additional ingredients. The DMEM high glucose medium contains L-Alanine 9mg/L, L-Asparagine Anhydrous 50mg/L, L-Aspartic acid 20mg/L, LGlutamic acid 20mg/L, L-Hydroxy-L-proline 20mg/L, L-Proline 34.5mg/L, Cupric Sulfate Pentahydrate 0.0025mg/L, Ferrous Sulfate Heptahydrate 0.834mg/L, Sodium Phosphate Dibasic Anhydrous 142.04mg/L, Zinc Sulfate Heptahydrate 0.863mg/L, D-Biotin 0.2mg/L, P-Aminobenzoic Acid(PABA) 1mg/L, Vitamine B12 1.36mg/L, Hypoxanithine 4.08mg/L, L-Glutathione Reduced 1mg/L, Linoleic acid 0.084mg/L, Putrescine+2HCL 0.161mg/L, Thioctic Acid 0.21mg/L, and Thymindine 0.73mg/L.
    • 目的:提供间充质干细胞的基础培养基,以提高干细胞增殖率,缩短培养时间。 构成:间充质干细胞的基础培养基ABM-M(高级碱性介质 - 间充质干细胞)具有基本的DMEM高葡萄糖培养基,并含有其他成分。 DMEM高糖培养基含有L-丙氨酸9mg / L,L-天冬酰胺无水50mg / L,L-天冬氨酸20mg / L,谷氨酸20mg / L,L-羟基-L-脯氨酸20mg / L,L-脯氨酸34.5 mg / L,硫酸铜五水合物0.0025mg / L,硫酸亚铁七水合物0.834mg / L,无水磷酸二氢钠142.04mg / L,硫酸锌七水合物0.863mg / L,D-生物素0.2mg / L,对氨基苯甲酸 PABA)1mg / L,维生素B12 1.36mg / L,羟虫硝酸4.08mg / L,L-谷胱甘肽降低1mg / L,亚油酸0.084mg / L,腐胺+ 2HCL 0.161mg / L,硫酸0.21mg / L, 胸腺嘧啶0.73mg / L。
    • 8. 发明公开
    • 연골세포 조기배양을 위한 연골세포 특이적 배양방법
    • 用于细胞培养细胞的特殊培养基及其使用方法
    • KR1020100036773A
    • 2010-04-08
    • KR1020080096153
    • 2008-09-30
    • 세원셀론텍(주)
    • 서동삼이준근고창권장동일이은영최민정장정호
    • C12N5/07C12N5/071C12N5/02C12N5/00
    • PURPOSE: A chondrocyte-specific culture medium for early culture of chondrocytes and a culture method are provided to enhance proliferation rate of chodrocytes isolated from cartilage tissue and shorten transplantation time. CONSTITUTION: A chondrocyte-specific culture method for early culture of chondrocytes comprises: a step of preparing DR in which DMEM medium is mixed in a ratio of 1:1; a step of adding component having higher concentration when same component is contained comparing DMEM and RPMI-1640; a step of making ABM-C(Advanced Basic Media(ABM)-Chondrocyte) medium; a step of culturing chondrocytes using the ABM-C medium or short-term chondrocytes using the ABM-C medium; and a step of culturing chondrocytes using ABM-C medium.
    • 目的:提供软骨细胞早期培养的软骨细胞特异性培养基和培养方法,以提高从软骨组织中分离的细胞的增殖率,缩短移植时间。 构成:用于软骨细胞早期培养的软骨细胞特异性培养方法包括:制备其中DMEM培养基以1:1的比例混合的DR的步骤; 比较DMEM和RPMI-1640时,添加相同成分时含有较高浓度的成分的步骤; 制作ABM-C(高级碱性介质(ABM) - 软骨细胞)培养基的步骤; 使用ABM-C培养基或使用ABM-C培养基的短期软骨细胞培养软骨细胞的步骤; 以及使用ABM-C培养基培养软骨细胞的步骤。