Bone marrow cell culture medium
A technology for bone marrow cells and culture medium, which is applied in bone/connective tissue cells, animal cells, culture process, etc., can solve the problems of few analyzable split images, high cost, complicated preparation process, etc., and achieves good shape and dispersion, Easy to observe, split the effect of many phases
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Embodiment 1
[0046] The preparation of embodiment 1 bone marrow cell culture medium
[0047] Serum, antibiotics were added to the basal medium. Wherein the basal medium is RPMI-1640 basal medium, and the concentration of each component is as follows:
[0048] Penicillin 100ug / ml
[0049] Streptomycin 50ug / ml
[0050] Solid Serum Replacement 1g / L
[0051] At the same time, the basal medium also contains glutamine, and the concentration of glutamine in it is 3mmol / L.
Embodiment 2
[0052] Embodiment 2 bone marrow cell culture
[0053] Bone marrow cells were cultured according to the following method, and the cultured cells were used for chromosome preparation. The steps that described method comprises are:
[0054] (1) Preparation of bone marrow cell culture medium: configure according to the components and dosages described in Example 1;
[0055] (2) Kind of bone marrow: Inoculate 0.5ml of bone marrow cell puncture solution into a glass or plastic bottle containing 10ml of medium in step (1), and gently rotate the culture tube to mix;
[0056] (3) Cultivation: place the culture medium inoculated with bone marrow cells in a carbon dioxide incubator at 37 degrees Celsius for cultivation, and the cultivation time is 72 hours;
[0057] (4) Terminate the culture: add colcemid with a final concentration of 0.1 ug / ml to the culture medium, and let stand for 15-30 minutes to terminate the culture.
Embodiment 3
[0058] Example 3 Bone marrow cell chromosome preparation
[0059] Carry out bone marrow cell chromosome preparation according to the following method, and the prepared cells are used for chromosome karyotype analysis. The steps that described method comprises are:
[0060] (1) Cell collection: transfer the cells terminated in Example 2 to a centrifuge tube, and remove the supernatant after centrifugation for 5 minutes under the action of a centrifugal force of 500 g to collect the cells;
[0061] (2) Hypotonic treatment: add 5-10ml of 0.075M KCL solution to the cells collected in step (1) to suspend the cells, and incubate at 37 degrees Celsius for 10-12 minutes;
[0062] (3) Centrifugation: centrifuge the cell suspension after the hypotonic treatment in step (2), and discard the supernatant after centrifugal force of 500g for 5 minutes;
[0063] (4) Fixation: Add 5-10ml of freshly prepared, pre-cooled acetic acid:methanol=1:3 fixative to the centrifuge tube, and fix at 4°C fo...
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Abstract
Description
Claims
Application Information
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