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    • 2. 发明授权
    • Dispenser for dried biological reagent spheres
    • 干生物试剂球的分配器
    • US5616299A
    • 1997-04-01
    • US469050
    • 1995-06-06
    • David W. WalkerBrent A. BurdickJames F. JollyDaniel D. Zender
    • David W. WalkerBrent A. BurdickJames F. JollyDaniel D. Zender
    • B01L99/00G01N35/00B01L11/00B65G29/00
    • B01L99/00B01J2219/00468G01N2035/00574
    • An apparatus for dispensing reagent spheres from a vial includes a housing with an inlet through which the reagent spheres are received from the vial. Within the housing is a dispensing tube which forms a passageway for the reagent spheres and which has a first relatively large section in communication with the inlet and a funnel section in which the passageway reduces in cross section to a narrower linearizing section. The cross sectional area of the linearizing section is only slightly larger than one of the reagent spheres being dispensed. A metering shaft extends across and blocks the linearizing section of the passageway. The metering shaft has a depression for conveying one reagent sphere at a time between portions of linearizing section when the metering shaft is rotated 180 degrees. A gear on the metering shaft meshes with teeth on a plunger which is slidably mounted to the housing. A user pressing the plunger causes the metering shaft to rotate transferring a reagent sphere to a portion of the passageway connected to the outlet of the housing and thereby ejects that reagent sphere from the housing.
    • 用于从小瓶分配试剂球的装置包括具有入口的壳体,试剂球从小瓶接收。 在壳体内部是分配管,其形成用于试剂球的通道,并且其具有与入口连通的第一相对大的部分和漏斗部分,其中通道在横截面上减小到较窄的线性化部分。 线性化部分的横截面面积仅略微大于被分配的一种试剂球体。 计量轴延伸穿过并阻塞通道的线性化部分。 计量轴具有用于当计量轴旋转180度时一次在线性化部分的部分之间输送一个试剂球的凹陷。 计量轴上的齿轮与可滑动地安装在壳体上的柱塞上的齿啮合。 按压柱塞的使用者使得计量轴旋转,将试剂球转移到连接到壳体出口的通道的一部分,从而将该试剂球从壳体喷出。
    • 6. 发明授权
    • Method of making double-stranded DNA sequences
    • 制作双链DNA序列的方法
    • US5132215A
    • 1992-07-21
    • US244871
    • 1988-09-15
    • Krishna JayaramanBrent A. BurdickFred T. Oakes
    • Krishna JayaramanBrent A. BurdickFred T. Oakes
    • C12P21/00C07K14/80C12N15/10C12Q1/68
    • C12N15/10C07K14/80C12Q1/6806C12Q1/686
    • A method of synthesizing double-stranded DNA sequences is disclosed. The method comprises the steps of:(a) preparing a first series of oligodeoxyribonucleotide fragments which, when joined in proper sequence, form a DNA coding strand;(b) preparing a second series of oligodeoxyribonucleotide fragments which, when joined in proper sequence, form a DNA strand complementary to the coding strand;(c) compelling hydrogen bonding and ligation in proper sequence between the first and second series of oligodeoxyribonucleotide fragments prepared in steps (a) and (b) in a single reaction to produce the entire double-stranded DNA sequence;(d) treating the double-stranded DNA sequence with one oligonucleotide primer for each strand under hybridizing conditions;(e) polymerizing an extension product of each primer that is complementary to each strand of the double-stranded DNA sequence which is a template for forming the primer extension product;(f) denaturing the product of step (e) to separate the primer extension products from their respective templates to form four separate single-stranded DNA sequences;(g) treating the denatured product of (f) with oligonucleotide primers, such that a primer extension product is synthesizing using each of the single strands produced in step (f) as a template resulting in amplification of the double-stranded DNA sequence; and(h) repeating steps (d), (e), (f) and (g) until the desired quantity of the double-stranded DNA sequence is formed.