膜联蛋白
碘化丙啶
细胞凋亡
异硫氰酸荧光素
哈卡特
流式细胞术
分子生物学
磷脂酰丝氨酸
重组DNA
化学
膜联蛋白A5
生物化学
荧光
生物
程序性细胞死亡
体外
磷脂
膜
物理
量子力学
基因
作者
Saeideh Sadat Shobeiri,Mojtaba Sankian
出处
期刊:Protein and Peptide Letters
[Bentham Science Publishers]
日期:2022-06-20
卷期号:29 (9): 806-814
被引量:5
标识
DOI:10.2174/0929866529666220617153809
摘要
Annexin V, a member of calcium-dependent phospholipid-binding proteins, selectively binds to the exposed phosphatidylserine, which can be used for in vitro apoptosis detection. Simultaneous staining of cells with annexin V-fluorescein isothiocyanate (FITC) and the non-vital dye propidium iodide (PI) enables the detection of apoptotic and necrotic cells.Our study aimed to express, purify, and stabilize the recombinant annexin V.The recombinant annexin V was cloned and expressed in E. coli bacteria and was purified using Ni-IDA resin. The FITC conjugation was performed, and apoptosis detection of HaCaT cells by FITC-labeled annexin V was evaluated by flow cytometry. Then, the stability of FITC-labeled annexin in various conditions, including polyvinyl alcohol (PVA), glycerol, and trehalose, was evaluated.The results showed that annexin V was appropriately expressed and purified. After FITC conjugation, it could perfectly detect the cell death of HaCat cells in different apoptosis percentages. FITC-labeled annexin had more stability with PVA than glycerol and trehalose.It seems that PVA has an acceptable effect on FITC-labeled annexin V stability in concentrations lower than 1 mg mL-1 without interfering with fluorescent intensity.
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