Sample collection, preparation and storage

RT Renyang Tong
LL Lingjie Luo
YZ Yichao Zhao
MS Mingze Sun
RL Ronghong Li
JZ Jianmei Zhong
YC Yifan Chen
LH Liuhua Hu
ZL Zheng Li
JS Jianfeng Shi
YL Yuyan Lyu
LH Li Hu
XG Xiao Guo
QL Qi Liu
TS Tian Shuang
CZ Chenjie Zhang
AY Ancai Yuan
LS Lingyue Sun
ZZ Zheng Zhang
KQ Kun Qian
LC Lei Chen
WL Wei Lin
AC Alex F. Chen
FW Feng Wang
JP Jun Pu
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Peripheral venous blood samples were collected in Vacutainer CPT (362761, BD, San Diego, CA, US) tubes and coagulation promoting tubes at four time points, including the day before vaccination (BV), 7 days after the first dose (1V7), 7 days after the second dose (2V7) and 14 days after the second dose (2V14). The blood samples were processed in 2 h after collection. The PBMCs were isolated using Vacutainer CPT tubes according to the manufacturer’s protocol [23]. The viability of PBMCs in each sample was confirmed to be >90% by Trypan Blue staining. PBMCs were immediately used for scRNA library construction and sequencing, or were cryopreserved at −80°C in 10% dimethylsulfoxide in fetal bovine serum. Blood samples in the coagulation promoting tubes were incubated upright for 20 min at 4°C. Then, the coagulation promoting tubes were centrifuged at 1000 × g for 10 min at 4°C. The supernatant serum in each tube was extracted and stored at −80°C for future assays.

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