做细胞爬片的免疫荧光染色,bsa封闭后,敷一抗时怎么处理啊?2
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发布时间:2023-10-14 08:53
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时间:2024-12-12 12:43
1. Dilute your primary antibody in your blocking buffer
2. Incubate your coverslips with primary antibody for 1 hours at room temperature or 4 degrees overnight
3. wash 3x PBS
4.your sample is ready for secondary antibody