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    • 63. 发明申请
    • SUBSTRATES FOR ISOLATING, REACTING AND MICROSCOPICALLY ANALYZING MATERIALS
    • 分离,反应和微观分析材料的基材
    • WO2004018623A3
    • 2004-04-15
    • PCT/US0325685
    • 2003-08-18
    • CLINICAL MICROARRAYS INCMONTAGU JEAN IDOWD ROGERROOT DAVID
    • MONTAGU JEAN IDOWD ROGERROOT DAVID
    • G01N1/28C40B40/06C40B40/10C40B60/14G01N21/64G01N33/58G01N37/00G01N33/543
    • G01N21/6452B01J2219/00315B01J2219/00387B01J2219/00533B01J2219/00605B01J2219/00612B01J2219/00637B01J2219/00641B01J2219/00722B01J2219/00725B01J2219/0074C40B40/06C40B40/10C40B60/14G01N21/274G01N21/6428G01N21/6456G01N33/54393G01N33/582
    • An immobilizing device for biological material comprises a rigid support (12) carrying a substrate layer (20, 20') of polymer having biological immobilizing properties, e.g. for amino and nucleic acids. Substantially solid ultra-thin substrate layers (20') having a thickness less than about 5 micron, preferably between about 0.1 and 0.5 micron, and micro-porous, ultra-thin substrate layers (20') having a thickness less than about 5 micron, preferably less than 3 micron, 2 or 1 micron are shown, which may be segmented by isolating moats M. The substrate layer is on a microscope slide (302), round disc (122), bio-cassette, at the bottom of a well of a multiwell plate, and as a coating inside a tube. Fluorescence or luminescence intensity and geometric calibration spots (420) are shown. Reading is enhanced by the intensity calibration spots (420) to enable normalization of readings under uneven illumination conditions, as when reading by dark field, side illumination mode. The reference spots are shown being printed simultaneously with printing an array of biological spots or with the same equipment. Methods of forming layers of the device include controlled drawing from a bath of coating composition and drying, and spinning of C-D shaped substrates. Post-forming treatment is shown by corona treatment and radiation. Adherent metal oxides (14), silica-based materials and other materials are used to unite layers of the composite. In multiwell plates the oxide promotes joining of a bottom plate (95, 95') and upper, well-defining structure (94) of dissimilar material. The oxides (14) also provide beneficial opacity to prevent light entering the glass support, for applying potential to the substrate, etc.
    • 用于生物材料的固定装置包括承载具有生物固定性质的聚合物的基底层(20,20')的刚性支撑体(12),例如。 用于氨基和核酸。 具有厚度小于约5微米,优选约0.1至0.5微米的基本上固体的超薄基底层(20')和厚度小于约5微米的微孔超薄基底层(20') ,优选小于3微米,2或1微米,其可以通过隔离护墙M分段。基底层在显微镜载玻片(302),圆盘(122),生物盒,底部 多孔板,以及管内的涂层。 显示荧光或发光强度和几何校准点(420)。 通过强度校准点(420)来增强读数,以使得在不均匀照射条件下的读数正常化,如通过暗场,侧面照明模式读取。 参考点被显示为同时印刷生物斑点阵列或用相同的设备打印。 形成装置层的方法包括从涂料组合物的浴中进行控制拉伸和干燥,以及C-D形基材的纺丝。 后处理通过电晕处理和辐射显示。 使用粘附金属氧化物(14),二氧化硅基材料和其他材料来组合复合材料层。 在多孔板中,氧化物促进底板(95,95')和不同材料的上部,良好限定结构(94)的接合。 氧化物(14)还提供有益的不透明性,以防止进入玻璃载体的光,将电位施加到基底等。