146 results about "Normal laboratory" patented technology

The invention relates to a microtube device and a using method thereof. The microtube device is characterized by comprising an upper layer of top cap layer and a lower layer of substrate layer, wherein the top cap layer is tightly connected with the surface of the substrate layer; the top cap layer and / or the substrate layer are / is provided with a branch microtube; the branch microtube consists of at least one activity screening tube, a buffer cavity and at least two branch tubes which are symmetrically distributed to the center of the buffer cavity; the buffer cavity is connected with the activity screening tube and the branch tube; meanwhile, the top cap layers corresponding to all the end positions of the branch microtube are provided with a hole respectively to form a sample inlet pool and a sample outlet pool; the sample inlet pools are communicated with the corresponding activity screening tube respectively; and the sample outlet pools are communicated with the corresponding branch tubes respectively. Cells can be cultured in situ in the sample outlet pool and can continuously generate a chemotactic matter by selectively adding cells capable of releasing the chemotactic matter into one or more sample outlet pools, so that uniform and stable chemical gradient fields are generated in the buffer cavity and the branch tubes. The microtube device has the advantages of simple manufacturing steps, low cost, quick and effective screening process, and easy popularization and use in ordinary laboratories.

The invention relates to a method for germinating ganoderma spores. The method comprises the following steps that ganoderma fruiting bodies having white sides on pileus and just starting to shoot spores are selected for collecting the spores; the spores are collected through a fruiting body movable cap bag; and the spores are applied on a germination culture medium (a prescription is as follows: 200ml of wort, 100ml of ganoderma lucidum extract, 20g of agar, 700ml of water, and sterilization is carried out for 30 minutes at 121DEG C), and a ganoderma mononuclear strain is obtained. The difficult problems that mature ganoderma spores are not easily germinated under laboratory conditions and the crossbreeding of ganoderma is difficult are solved. The method for germinating ganoderma spores is simple and feasible, no special medicine, instruments and equipment need to be used, and the required mononuclear strain for crossbreeding or the genetic analysis of ganoderma can be obtained in an ordinary laboratory.