Multi-hole cell culture dish structure

Abstract

The present invention provides a multi-hole cell culture dish structure. With the multi-hole cell culture dish structure, a plurality of cells can be independently cultured in a culture dish so as to save equipment cost, and an operation time is short and efficiency is high during culture. The multi-hole cell culture dish structure comprises a cell culture dish, and is characterized in that the bottom surface of the cell culture dish is provided with uniformly-distributed small hole grooves, glass sheets are correspondingly placed in the small hole grooves, adjacent positions of the small hole grooves are provided with strip grooves, both sides of the single strip diameter of the small hole groove are provided with columns, the column is prepared from a hot melting material, and corresponding positions of every small hole groove are marked with different numbers.

Description

technical field [0001] The invention relates to the technical field of cell culture devices, in particular to the structure of a porous cell culture dish. Background technique [0002] The glass bottom cell culture dish can be used for cell culture observation experiments such as laser confocal microscopy experiment, fluorescence microscopy experiment and phase contrast microscopy experiment, and can also be used for the observation of living cells, but the existing glass bottom culture dish has only one container. Cells can be cultured once, resulting in the need to culture multiple independent cells requiring multiple glass-bottom cell culture dishes, which increases equipment costs, and the operation time of culture is long and the efficiency is low. Contents of the invention [0003] In view of the above problems, the present invention provides a structure of a porous cell culture dish, which allows a plurality of cells to be cultured independently in one vessel, saves...

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Problems solved by technology

[0002] The glass bottom cell culture dish can be used for cell culture observation experiments such as laser confocal microscopy experiment, fluorescence microscopy experiment and phase contrast microscopy experiment, and can also be used for the observation of living cells, but the existing glass bottom culture dish has only one container. Cells can be cultured once, resulting in the need to culture multiple independent cells requiring multiple glass-bottom cell culture dishes, which increases the cost of equipment, and the operation time of culture is long and the efficiency is low

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