An automatic configuration device for biological laboratory culture medium
An automatic configuration, laboratory technology, applied in biochemical cleaning devices, enzymology/microbiology devices, biomass post-processing, etc., can solve the problems of difficult application of commercially available filling machines and insufficient accuracy of commercially available filling machines , to achieve the effect of eliminating repetitive labor, avoiding pollution, and ensuring uniformity
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Embodiment 1
[0040] This example provides a process for the laboratory to automatically configure LB culture medium. LB medium is one of the most commonly used media in microbiology laboratories. In this example, the experimenter needs to configure LB medium. According to the "Molecular Cloning Experiment Guide", 1L liquid LB medium should be added to 950ml deionized water: 10g tryptone, 5g yeast extract, 10g NaCl, adjust pH to 7.0 with 5mol / L NaOH, and dilute to 10g with deionized water. 1L.
[0041] When using the present invention to prepare the LB medium, the experimenter turns on the machine, such as figure 1 As shown, click Start in the 2-Control panel, then select common medium, and then select LB medium, the panel will display: Please put tryptone in No. 1 feeding port, and put yeast extract in No. 2 feeding port, No. 3 feeding port is put into NaCl. Experimenters add each raw material as required, and the quality of the added raw material must exceed the required amount. The ...
Embodiment 2
[0047] This example provides the process of automatically configuring the phenylalanine medium in the laboratory. To configure 1L liquid phenylalanine medium, add in 950ml deionized water: yeast extract 3g, L-phenylalanine 2g, disodium hydrogen phosphate 1g, NaCl 5g, agar 12g, adjust pH to 5mol / L NaOH 7.0, make up to 1L with deionized water.
[0048] It is assumed that the phenylalanine medium is not written in the usual medium in the procedure of the present invention. When using the present invention to prepare the phenylalanine medium, the experimenter turns on the instrument, selects the custom mode, and inputs 3g for the No. 1 feeding port, 2 g for the No. 2 feeding port, 1 g for the No. 3 feeding port, 5 g for the No. 4 feeding port, and No. 5 feeding port. Feeding port 12g. The experimenter clicks start and the instrument starts running. The subsequent steps were the same as in Example 1.
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