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[backcolor=rgba(255, 255, 255, 0.8)]Fixed specimens at an optimal concentration were placed onto a 400-mesh carbon/formvar coated grids and allowed to absorb to the formvar for a minimum of 1 min. For immunogold staining the grids were placed into a blocking buffer for a block/permeabilization step for 1 h. Without rinsing, the grids were immediately placed into the primary antibody at the appropriate dilution overnight at 4 °C (1:300 anti-CD9 ab92726, Abcam and anti-GPC1 PIPA528055, Thermo Scientific). [backcolor=rgba(255, 255, 255, 0.8)]As controls, some of the grids were not exposed to the primary antibody. [backcolor=rgba(255, 255, 255, 0.8)]The next day, all the grids were rinsed with PBS then floated on drops of the appropriate secondary antibody attached with 10-nm gold particles (AURION) for 2 h at room temperature. [backcolor=rgba(255, 255, 255, 0.8)]Grids were rinsed with PBS and were placed in 2.5% glutaraldehyde in 0.1 M phosphate buffer for 15 min. After rinsing in PBS and distilled water the grids were allowed to dry and stained for contrast using uranyl acetate.[backcolor=rgba(255, 255, 255, 0.8)]
固定标本的最佳浓度被放置到一个400 -网状碳/ formvar涂层网格和允许吸收formvar染色然后至少1分钟。为电镜观察,网格被放到一个阻塞缓冲块/透化作用的步骤1 h。无需冲洗,网是立即放入一抗在适当的稀释在4°C过夜(anti-CD9 ab92726,Abcam和anti-GPC1 PIPA528055,热科学)。作为对照[backcolor=rgba(255, 255, 255, 0.8)],一些网格没有暴露于一抗。[backcolor=rgba(255, 255, 255, 0.8)]第二天,所有的网格用PBS冲洗,然后孵育适当的二次抗体滴附有soi黄金粒子在室温下(AURION)2h。[backcolor=rgba(255, 255, 255, 0.8)]网格冲洗PBS和放置在0.1 2.5%的戊二醛磷酸缓冲15分钟。在PBS和蒸馏水冲洗后网格被允许干和彩色对比使用醋酸双氧铀。
[backcolor=rgba(255, 255, 255, 0.8)]求做过的大神来指点下~~ 他这是因为要胶体金标记,所以才孵育抗体的吧?醋酸双氧铀负染一般不用一抗、二抗的步骤吧?正准备做,求大神指点
来源文献:
Glypican-1 identifies cancer exosomes and detects early pancreatic cancer .2015.nature
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