Jiang Ling-xiao, Guo Zhao-biao, Chen Ze-liang, Wang Jin, Wazng Hong-xia, Yu Shou-yi, Yang Rui-fu
Department of Epidemiology, Southern Medical University, Guangzhou 510515, China.
Di Yi Jun Yi Da Xue Xue Bao. 2004 Nov;24(11):1230-2.
To define the optimal conditions for preparing protein chips on aldehyde-coated slides.
The proteins were diluted in PBS containing 40% glycerol and spotted on aldehyde-coated slides. After the spots were dried for 1 hour at room temperature, the slides were stored at 4 degrees Celsius;. Following block and rinse, the slides were used for immunoassay and the results detected with a scanner. Several key factors that might influence the results were tested, including the number of spots, concentration of protein in the spotting solution, time of immobilization and the blocking reagent.
Pre-spotting of 10 to 15 spots achieved good homogeneity of the subsequent spots on aldehyde-coated slides. The protein immobilized at 4 degrees Celsius; for 24 to 48 h showed higher fluorescence intensity and clearer images, and the slides blocked with 3% BSA produced the lowest background signal. The concentration of protein in the spotting solution significantly affected the fluorescence intensity.
To ensure good results in preparing protein chips on aldehyde slides, pre-spotting of 10-15 spots can be necessary followed by immobilization at 4 degrees Celsius; for 24-48 h and 3% BSA blocking.
确定在醛基包被载玻片上制备蛋白质芯片的最佳条件。
将蛋白质用含40%甘油的磷酸盐缓冲盐水(PBS)稀释后点样于醛基包被载玻片上。室温下斑点干燥1小时后,载玻片于4摄氏度保存。封闭和冲洗后,载玻片用于免疫测定,结果用扫描仪检测。测试了几个可能影响结果的关键因素,包括斑点数量、点样溶液中蛋白质浓度、固定时间和封闭剂。
预先点样10至15个斑点可使醛基包被载玻片上后续斑点具有良好的均匀性。在4摄氏度固定24至48小时的蛋白质显示出更高的荧光强度和更清晰的图像,用3%牛血清白蛋白(BSA)封闭的载玻片产生的背景信号最低。点样溶液中蛋白质浓度显著影响荧光强度。
为确保在醛基载玻片上制备蛋白质芯片取得良好结果,可能需要预先点样10 - 15个斑点,然后在4摄氏度固定24 - 48小时并用3% BSA封闭。