Fixation fluid for saving cast-off cells and manufacturing method of cell shallow layer smear
A technology for exfoliating cells and a production method, applied in the field of cell preservation fixative, can solve the problems of unfavorable observation and diagnosis, long production time, and high machine cost, and achieve the effects of being beneficial to observation and diagnosis, reducing price, and reducing impurities
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Embodiment 1
[0028] Example 1: Preparation of Cell Preservation Fixative
[0029] The reagents used below are all chemically pure.
[0030] Get 10ml of methanol with a volume concentration of 99%, 15ml of ethanol with a volume concentration of 100%, 2ml of glycerol with a volume concentration of 99%, 2ml of polyethylene glycol with a molecular weight of 180, 10ml of formaldehyde with a volume concentration of 37%, 0.5 1 ml of glacial acetic acid with a volume concentration of 100%, 10 ml of sodium chloride with a mass concentration of 0.9%, and 68.5 ml of phosphate buffer solution with a pH value of 6.3 are uniformly mixed to obtain the exfoliated cell preservation fixative of the present invention.
[0031] Tinpreper TCT manufacturers
Embodiment 2
[0032] Example 2: Preparation of Cell Preservation Fixative
[0033] The reagents used below are all analytically pure.
[0034] Take 15ml of methanol with a volume concentration of 99%, 15ml of ethanol with a volume concentration of 99%, 1ml of glycerol with a volume concentration of 99%, 2ml of polyethylene glycol with a molecular weight of 200, 12ml of formaldehyde with a volume concentration of 40%, 1ml Glacial acetic acid with a volume concentration of 99%, 20ml of sodium chloride with a mass concentration of 0.85%, and 34ml of phosphate buffer solution with a pH value of 6.5 were evenly mixed to obtain the exfoliated cell preservation fixative of the present invention.
Embodiment 3
[0035] Embodiment 3: the making method of cell thin layer smear
[0036] 1) Place the collected sample in 10 ml of the exfoliated cell preservation solution described in Example 2 and shake for 20 minutes, then let it stand for 10 minutes and then pour it into a centrifuge tube at 2000 rpm for 8 minutes;
[0037] 2) Pour off the supernatant until the residue in the centrifuge tube is 1-2ml, then shake it well to obtain the cell suspension;
[0038] 3) Take 0.5ml of the cell suspension and put it into a film-making cup, and use a cell film-making machine containing filter paper with a 100-mesh filter screen stuck to the hollow part to make a thin-layer smear of cells.
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