Method using umbilical cord tissue cryopreservation to preserve various stem cells, thawing method and application
A cryopreservation method and technology of umbilical cord tissue, applied in the field of life sciences, can solve the problems of affecting the effect of cryopreservation and high tissue water content, and achieve the effects of program-controlled cooling and cryopreservation process fast, improving utilization rate and improving effect
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Embodiment 1
[0041] Umbilical cord tissue cryopreservation method of the present invention is as follows:
[0042] First, separate the frozen umbilical cord tissue into Wharton's jelly, wash the umbilical cord fully with normal saline in a cell culture dish, cut off the two ends of the umbilical cord with tissue scissors, and then rinse; Cut the umbilical cord into small pieces with scissors and clean them; then cut a small opening in each small piece of umbilical cord along the direction parallel to the veins, then tear it longitudinally with tissue forceps and flatten it; then carefully peel off the blood vessels and amniotic membrane from the umbilical cord, The part of Wharton's Jelly was fully washed 3 times with normal saline, and cut to 1-2 cm 3 small pieces.
[0043] One tissue block was reserved for the stripped Wharton's jelly tissue as a control experiment. The control experiment consisted of three parts: 1. Take a piece of fresh tissue and fix it in 10% neutral formalin, send...
Embodiment 2
[0079] The cryopreservation experiment of umbilical cord Wharton jelly tissue was carried out by using the formula of the cryopreservation agent of the No. 5 experimental group in the proportion of DMSO content in the cryopreservation solution added with fetal bovine serum (FBS) in Table 1.
[0080] A section of umbilical cord was selected, and the separation and pretreatment process of the umbilical cord Wharton's jelly tissue was carried out according to the method in Example 1, and one part was reserved as a control test group. The rest were evenly divided into 15 cryopreservation tubes, and the cryopreservation agent of No. 5 experimental group was added, and each 5 cryopreservation tubes were regarded as a group, and the program controlled cooling and freezing were carried out.
[0081] One group adopts a program-controlled cooling and freezing program: keep at 3°C for 4 minutes; drop to -10°C at 2°C / min and keep for 12 minutes; drop to -50°C at 0.5°C / min and keep for 5 ...
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