Abstract:
Provided is a method for amplifying the nucleic acid of a cell by dissolving the cell specifically bonded to a solid support. By means of the same, without a separate step of isolating a cell specifically bonded to a solid support or the nucleic acid of the same, the nucleic acid can be amplified from the cell specifically bonded to the solid support.
Abstract:
Provided are: a composition or a kit for detecting nucleic acids containing genetic variation which comprises a first amplification inhibiting nucleic acid and a second amplification inhibiting nucleic acid; and a method for detecting nucleic acids containing genetic variation using the same. By using the composition or the method, nucleic acids comprising genetic variation can be detected with excellent sensitivity and accuracy.
Abstract:
By using a composition, a kit, or a method of separating cells using the same including a complex of at least one type of a linker capable of specifically binding to an antibody or antigen binding fragment and a complex of a solid support unit, cells can be effectively separated from a sample. Moreover, a disease can be diagnosed by detecting the separated cells.
Abstract:
The present invention relates to a method for separating a nucleic acid from cells, a composition for preventing the adsorption of a nucleic acid on the surface of a solid support, and a kit for separating a nucleic acid from cells. The method for separating a nucleic acid from cells comprises the steps of: incubating a sample and a solid support including cells, and attaching the cells on the solid support; making the solid support attached to the cells be suspended in a composition including alkali metal salts of 100-300 mM and having pH 6-8; and obtaining a nucleic acid from the solution obtained by lysis.
Abstract:
The present invention relates to a method of sequential and multiple immunostaining for detection of various antigens in the same specimens. The immunostaining method can be used for qualitative or quantitative analysis of proteins expressed, gene analysis, and morphological analysis even in specimens where only a small amount is available. Fluorescent pigments according to an embodiment of the present invention are selected from a group consisting of FITC, DAPI, Cy5, Cy3, Texas Red and Rhodamine.
Abstract:
The present invention relates to linker polypeptides, a composition or a kit comprising the same, and a method for analyzing a target material using the same. When the linker polypeptides are used, signal distortion which can be caused by micro-particles when analyzing a target material is prevented, thereby being useful for increasing accuracy and reliability of diagnosis. [Reference numerals] (AA) Fc-binding domain; (BB) TEV cutting domain; (CC) C-terminal modification
Abstract:
PURPOSE: A metal nanowire in which gold nanocluster is formed on the surface and a method of binding for the metal nanowire with target material are provided to efficiently bond with target material at high affinity. CONSTITUTION: A metal nanowire in which gold nanocluster is formed on the surface is existed in the composition form. The gold nanocluster has average size of 1-10 nano meters. The gold nanocluster is existed in the density range of 1X10^6 - 1X10^16clusters/cm^2. A manufacturing method of the metal nanowire comprises the following steps: forming a gold thin film layer on a metal board; forming gold - metal island by primary sintering the gold containing metal substrate in a chamber for chemical vapor deposition; and injecting mixing gas into the chamber while secondary sintering the silicon substrate to grow metal nanowire in which gold nanocluster is formed on the surface. [Reference numerals] (AA) Trapping rate(%); (BB) Culturing time(minutes)