Abstract: A continuous mining and delayed filling mining method for a deep ore body masonry structure is provided, comprising: dividing an ore body into ore blocks along a trend, internally dividing each ore block into stopes with square masonry structures, and reserving a rib pillar between the ore blocks; arranging an ore block conveyor belt gallery and a stope conveyor belt gallery at the lower parts of the ore blocks, arranging ore block crossheading and stope crossheading at the upper parts of the ore blocks, mining the stopes in the sequence from the foot wall to the hanging wall. In accordance with the present disclosure, adverse effects caused by deep high geo-stress and high geo-temperature on mining operation can be effectively overcome. The method has the advantages of low carbon and environmental protection, safety of recovery operation, high mechanization of stope operation, low labor intensity of manual operation and the like.

Abstract: A rock true triaxial dynamic compression-shear test equipment, and method under deep complex structure conditions, includes a counterforce framework, a pressure chamber, a base platform and four actuators. A pressure chamber transfer track is arranged on the base platform, and a pressure chamber transfer slipway is arranged on the tracks. The pressure chamber is a split structure. A pressure chamber base is located on the pressure chamber transfer slipway, and a pressure chamber barrel is provided with a pressure chamber barrel lift type bearing table and a pressure chamber barrel hoisting mechanism. The pressure chamber is provided with pressure chamber barrel and base packaging fixtures.

Abstract: The present invention relates to a rock true triaxial dynamic compression-shear test equipment and method under deep complex structure conditions. The device comprises a counterforce framework, a pressure chamber, a base platform and four actuators. Pressure chamber transfer tracks are arranged on the base platform, and a pressure chamber transfer slipway is arranged on the tracks. The pressure chamber is a split structure. A pressure chamber base is located on the pressure chamber transfer slipway, and a pressure chamber barrel is provided with a pressure chamber barrel lift type bearing table and a pressure chamber barrel hoisting mechanism. The pressure chamber is provided with pressure chamber barrel and base packaging fixtures.

Abstract: A lateral flow apparatus is provided.

Abstract: A lateral flow apparatus is provided.

Abstract: The proteins in a biological sample that is sought to be analyzed for its protein composition by an electrophoretic or chromatographic procedure are coupled to a dye in an unusually efficient manner by combining the sample with a solid dry composition containing the dye, a buffering agent, and in preferred embodiments, a denaturing agent as well. The solid and dry form of the composition prevents the dye from deteriorating or decomposing, and the combination of components in the composition allows the dye to couple to the proteins in a relatively uniform manner with no overstaining of the protein when the composition and the sample are heated together and held at an elevated temperature for a short period of time.

Abstract: Proteins and other analytes that have been separated by electrophoretic means in a gel are transferred to a membrane by conventional blotting techniques, the membrane being a composite of an analyte binding layer and a size retention layer. The pore size of the size retention layer is large enough to allow non-macromolecular ions to pass, yet not large enough to allow the passage of the analytes from the gel, nor antibodies or other macromolecules or reagents in general that might be used in the detection, imaging, or quantification of the analytes.

Abstract: The proteins in a biological sample that is sought to be analyzed for its protein composition by an electrophoretic or chromatographic procedure are coupled to a dye in an unusually efficient manner by combining the sample with a solid dry composition containing the dye, a buffering agent, and in preferred embodiments, a denaturing agent as well. The solid and dry form of the composition prevents the dye from deteriorating or decomposing, and the combination of components in the composition allows the dye to couple to the proteins in a relatively uniform manner with no overstaining of the protein when the composition and the sample are heated together and held at an elevated temperature for a short period of time.

Abstract: The proteins in a biological sample that is sought to be analyzed for its protein composition by an electrophoretic or chromatographic procedure are coupled to a dye in an unusually efficient manner by combining the sample with a solid dry composition containing the dye, a buffering agent, and in preferred embodiments, a denaturing agent as well. The solid and dry form of the composition prevents the dye from deteriorating or decomposing, and the combination of components in the composition allows the dye to couple to the proteins in a relatively uniform manner with no overstaining of the protein when the composition and the sample are heated together and held at an elevated temperature for a short period of time.

Abstract: The proteins in a biological sample that is sought to be analyzed for its protein composition by an electrophoretic or chromatographic procedure are coupled to a dye in an unusually efficient manner by combining the sample with a solid dry composition containing the dye a buffering agent, and in preferred embodiments, a denaturing agent as well. The solid and dry form of the composition prevents the dye from deteriorating or decomposing, and the combination of components in the composition allows the dye to couple to the proteins in a relatively uniform manner with no overstaining of the protein when the composition and the sample are heated together and held at an elevated temperature for a short period of time.

Abstract: The proteins in a biological sample that is sought to be analyzed for its protein composition by am electrophoretic or chromatographic procedure are coupled to a dye in an unusually efficient manner by combining the sample with a solid dry composition containing the dye, a buffering agent, and in preferred embodiments, a denaturing agent as well. The solid and dry form of the composition prevents the dye from deteriorating or decomposing, and the combination of components in the composition allows the dye to couple to the proteins in a relatively uniform manner with no overstaining of the protein when the composition and the sample are heated together and held at an elevated temperature for a short period of time.