会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 92. 发明授权
    • pK-matched running buffers for gel electrophoresis
    • 用于凝胶电泳的pK匹配运行缓冲液
    • US06582574B1
    • 2003-06-24
    • US09536392
    • 2000-03-28
    • Qiang LiuSteve S. Sommer
    • Qiang LiuSteve S. Sommer
    • B01D5702
    • C07K1/26G01N27/44747Y10S435/967Y10T436/108331
    • pK-matched buffers, each containing two effective buffering components: one weak base and one weak acid which have similar pKa at 25° C. (within 0.3 pK units On agarose gels, the buffers in various concentrations were tested for separation of double-stranded DNA fragments with various DNA markers, agarose gel concentrations, and field strengths. Mobility was inversely proportional to the logarithm of molecular weight. The buffers provided high resolution without smearing at more dilute concentration than is possible with standard TAE (Tris/Acetate, pH 8.0) or TBE (Tris/Borate, pH 8.3) buffers. The buffers were also tested in 7M urea denaturing LongRanger™ sequencing gels and in non-denaturing polyacrylamide SSCP gels. The pK-matched buffers provide good separation and high resolution, at a broad range of potential pH values. In comparison to TAE and TBE, pK-matched buffers provide higher voltage and current stability, lower working concentration, more concentrated stock solutions, and lower current per unit voltage, resulting in less heat generation.
    • pK匹配的缓冲液,每个含有两个有效的缓冲组分:一个弱碱和一个在25℃具有相似pKa的弱酸(在0.3 pK单位内)在琼脂糖凝胶上,测试各种浓度的缓冲液分离双链 具有不同DNA标记的DNA片段,琼脂糖凝胶浓度和场强,迁移率与分子量的对数成反比。缓冲液提供高分辨率,不会在比标准TAE(Tris /醋酸盐,pH 8.0)下更浓的浓度 )或TBE(Tris /硼酸盐,pH 8.3)缓冲液,还在7M尿素变性LongRanger TM测序凝胶和非变性聚丙烯酰胺SSCP凝胶中测试缓冲液,pK-匹配的缓冲液提供良好的分离和高分辨率 与TAE和TBE相比,pK匹配缓冲液提供更高的电压和电流稳定性,更低的工作浓度,更集中的储备溶液, 并降低每单位电压的电流,导致较少的发热量。
    • 93. 发明申请
    • Dual-filled twin bag, a package and a method for forming a package for administering a solution
    • 双填充双袋,包装和用于形成用于施用溶液的包装的方法
    • US20030114788A1
    • 2003-06-19
    • US10283654
    • 2002-10-29
    • Michael R. KeilmanWalter A. MakarykJoseph A. Giertych
    • A61M001/00
    • A61M1/28A61J1/00A61M1/1668A61M1/1686Y10S128/24Y10S206/828Y10T436/108331
    • A dual-filled twin bag, a packaging including the twin bag, and a method for forming the packaged twin bags are provided. Each of two bags, a solution bag (10) and a drain bag (12) for a system used for a peritoneal dialysis procedure, are filled, at least partially, with a solution (14). A tubing set (16) connects the two filled bags (10,12) and may also be filled with solution (14) which is added to the bags (10,12) and the tubing set (16) during the manufacturing process. Alternatively, the tubing set (16) may be filled with air. The tubing set (16) is sandwiched between the solution bag (10) and the drain bag (12) and subsequently packaged in an overpouch (24). The method for forming the package including the bags filled with solution is simplified and the overall package size is reduced due to the sandwiched tubing set (16) between the solution bags (10,12) and the provision of solution in both bags (10,12).
    • 提供双填充双袋,包括双包的包装以及用于形成包装的双袋的方法。 至少部分地用溶液(14)填充两个袋子中的每个袋,溶液袋(10)和用于腹膜透析程序的系统的排液袋(12)。 管道组(16)连接两个填充的袋(10,12),并且还可以在制造过程中填充有添加到袋(10,12)和管组(16)中的溶液(14)。 或者,管组(16)可以填充空气。 管套(16)夹在溶液袋(10)和排放袋(12)之间,随后包装在一个外袋(24)中。 用于形成包括填充有溶液的袋的包装的方法被简化,并且由于溶液袋(10,12)之间的夹套管组(16)和在两个袋(10,12)中提供溶液,整体包装尺寸减小, 12)。
    • 94. 发明授权
    • Lytic reagent composition for determination of nucleated blood cells
    • 用于测定有核血细胞的溶血剂试剂组合物
    • US06573102B2
    • 2003-06-03
    • US09917530
    • 2001-07-27
    • Yi LiJing Li
    • Yi LiJing Li
    • G01N3100
    • G01N33/80G01N15/12G01N15/1459G01N33/5002G01N33/721G01N2015/1006G01N2015/1493Y10T436/10Y10T436/101666Y10T436/107497Y10T436/108331
    • A lytic reagent composition for measuring nucleated blood cells in a blood sample is described. The lytic reagent composition contains a quaternary ammonium surfactant, an ethoxylated phenol, and an ethoxylated alcohol. When mixed with a blood sample, the lytic reagent composition lyses red blood cells and enables a differentiation of nucleated red blood cells from other cell types by DC impedance measurement. The lytic reagent composition can further contain an organic ligand for determining total hemoglobin concentration of a blood sample photometrically. Further disclosed is a lytic reagent system including the lytic reagent composition and a diluent. In addition, a single reagent composition containing salts is also disclosed, which can be used without a separate diluent. The lytic reagent compositions can be used for concurrent measurement of nucleated red blood cells, WBC, and hemoglobin of a blood sample.
    • 描述了用于测量血液样品中的有核血细胞的溶解试剂组合物。 溶解试剂组合物含有季铵表面活性剂,乙氧基化苯酚和乙氧基化醇。 当与血液样品混合时,溶解试剂组合物溶解红细胞,并且通过DC阻抗测量使得有核红细胞与其它细胞类型分化。 溶解试剂组合物还可以含有用于测定血样的总血红蛋白浓度的有机配体。 还公开了包括溶解试剂组合物和稀释剂的裂解试剂系统。 此外,还公开了含有盐的单一试剂组合物,其可在没有单独的稀释剂的情况下使用。 裂解试剂组合物可用于同时测量血液样品的有核红细胞,WBC和血红蛋白。
    • 98. 发明申请
    • Recovering cryopreserved conifer embryogenic cultures
    • 回收冷冻保存的针叶树胚胎发生培养物
    • US20020192818A1
    • 2002-12-19
    • US09573160
    • 2000-05-19
    • Michael Ryan BecwarSharon Anne Krueger
    • C12N005/00C12N005/02
    • C12N5/0025C12N5/04Y10T436/108331
    • This invention relates to a method for improving the growth and regeneration potential of embryogenic cell and tissue cultures of coniferous plants retrieved from cryopreservation. In particular, this invention relates to the use of abscisic acid in the post-cryopreservation recovery medium to improve both the growth and somatic embryo production of embryogenic cell and tissue cultures of conifers, thereby enabling more rapid proliferation of the embryogenic cultures and a subsequent increase in the yield of somatic embryos. This method is well-suited for employment with a number of biotechnological uses of embryogenic cultures of coniferous plants retrieved from cryopreservation, including use with embryogenic cultures of coniferous plants and with genetically transformed embryogenic cultures of coniferous plants for producing clonal planting stock useful for reforestation.
    • 本发明涉及一种提高从冷冻保存回收的针叶植物胚胎发生细胞和组织培养物的生长和再生潜力的方法。 特别地,本发明涉及脱落酸在后冷冻保存回收培养基中的用途,以改善针叶树胚胎发生细胞和组织培养物的生长和体细胞胚胎产生,从而使胚胎发生培养物更快速增殖,并随后增加 体细胞胚的产量。 这种方法非常适合用于从冷冻保存中回收的针叶植物的胚胎发生培养物的许多生物技术用途,包括用于针叶植物的胚发生培养物和用于生产用于再造林的克隆种植原料的经遗传转化的针叶植物培养物。