Unlock instant, AI-driven research and patent intelligence for your innovation.

Cell culture dish and cell sampling method thereof

A cell culture and petri dish technology, which is applied in tissue cell/virus culture devices, biochemical equipment and methods, biochemical instruments, etc., can solve the problem of difficult screening of monoclonal cells, reduced screening success rate, low screening efficiency, etc. problem, to achieve the effect of improving the success rate of the experiment, shortening the experiment cycle, and improving efficiency

Active Publication Date: 2018-05-11
浙江奥比特生物科技有限公司
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Method 2, the screening efficiency is low, and there are often no cells or multiple clones in the culture well, and if the antibiotic screening process fails to kill all the untransfected cells, the screening success rate of this method is greatly reduced; in addition, if the transfection The above contradiction is more prominent when the efficiency is low, and it is difficult to screen out transfected monoclonal cells

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Cell culture dish and cell sampling method thereof
  • Cell culture dish and cell sampling method thereof
  • Cell culture dish and cell sampling method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] figure 1 It is a schematic diagram of the structure of a single well of a culture dish. The culture dish has various specifications and sizes, and there are 6 holes, 12 holes, 24 holes, 48 ​​holes, 96 holes and other specifications in terms of the number of culture holes. figure 1 Only one of the Petri dish wells is shown in . Such as figure 1 and figure 2 As shown, there are multiple concentric circles 13 and straight lines 12 passing through the centers of the concentric circles at the bottom of a single culture dish hole 10, and the concentric circles 13 and the straight lines 12 together form a positioning line. Such as figure 2 As shown, the bottom of the petri dish is divided into multiple regions by the concentric circles and cross lines. Assuming that the area of ​​the bottom surface of the petri dish is S, and assuming that the radii of the three concentric circles are a, b, and c respectively, the following relationship is satisfied: c = 2a, The radius...

Embodiment 2

[0056] The petri dish in this embodiment is basically the same as that in the first embodiment, except that the lengths of the protrusions and grooves on the holes of the petri dish and the sleeve are different from those in the first embodiment. In this embodiment, the first set of barrels is taken as an example for illustration, and the grooves and protrusions of the other sets of barrels are consistent with those of the first set of barrels.

[0057] Such as Figure 9 and Figure 10 As shown, the longitudinal protrusion 51 on the culture dish hole 50 does not completely penetrate the hole wall, that is to say, there is no protrusion structure on the upper part of the hole wall of the culture well 50 . The longitudinal groove 61 on the first set of barrels 60 runs through the barrel wall up and down, or is only distributed in the lower half of the set of barrels. There is no protruding structure in part, and the two can rotate relatively, and the position of the sampling h...

Embodiment 3

[0065] The culture dish and the sleeve in this embodiment can adopt the structure in Embodiment 1 or Embodiment 2.

[0066] The difference between this embodiment and the previous two embodiments is that there is a ring of protruding edges at the lower openings of the first sampling hole, the second sampling hole and the third sampling hole. Taking the third set of barrels 40 as an example, as Figure 11 As shown, the third sampling hole 41 extends downwards from a raised edge 43 . The protruding edges of the three sampling holes are used as supports to prevent the bottom of the barrel from damaging cells outside the sampling holes. At the same time, this ring of protrusions can separate the selected cell area from other areas. Prevent cell digestion fluid or cells from leaking out.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a cell culture dish and a cell sampling method thereof. The cell culture dish comprises a culture dish hole and sleeves, wherein the culture dish hole is used for culturing to-be-separated cells, the sleeves are placed into the culture dish hole during cell extraction to delimitate the cell extraction area of a target position, the sleeves include a first sleeve, a second sleeve and a third sleeve, the first sleeve is provided with a first sampling hole concentric with the first sleeve, the second sleeve is provided with a second sampling hole which deviates from the circle center of the second sleeve, and the third sleeve is provided with a third sampling hole located at the edge of the wall of the third sleeve. The cell culture dish has the advantages that the cell culture dish is provided with the three sleeves with different sampling hole positions, the target cells at different positions in the cell culture dish can be covered, and sampling purposiveness is increased.

Description

technical field [0001] The invention relates to a cell culture dish and a cell sampling method thereof, belonging to the field of biological experiment equipment. Background technique [0002] Cell transfection is a technique for introducing exogenous molecules such as DNA, RNA, etc. into eukaryotic cells. With the continuous development of molecular biology and cell biology research, transfection has become a routine tool to study and control gene function in eukaryotic cells. Transfected cells were passaged 72 hours after transfection and cultured with selection medium containing specific antibiotics. After a period of culture, the cells that failed to transfect the exogenous gene were killed, and a single cell could be seen in the culture dish. After continuing to culture, a single cell could divide and multiply to form a single resistant colony. At this time, two methods can be used to select a single clone: [0003] ①Filter paper method: Soak a sterilized 5x5mm filter...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C12M3/00C12M1/22C12Q1/24
CPCC12M23/10C12Q1/24
Inventor 唐明张翔
Owner 浙江奥比特生物科技有限公司