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同一载玻片上采用胶体金进行光镜与电镜免疫细胞化学对照研究。

Correlative light and electron microscopic immunocytochemistry on the same section with colloidal gold.

作者信息

Mar H, Tsukada T, Gown A M, Wight T N, Baskin D G

出版信息

J Histochem Cytochem. 1987 Apr;35(4):419-25. doi: 10.1177/35.4.3546488.

Abstract

Ultrastructural localization of growth hormone in rat anterior pituitary and of muscle-specific actin in rabbit arterial smooth muscle cells was accomplished with a post-embedment procedure using colloidal gold. Plastic sections (2 microns) were mounted on slides, deplasticized, immunostained with immunoglobulin-colloidal gold particles, re-embedded in Epon, and sectioned for electron microscopy. This procedure enabled light and electron microscopic localization of these intracellular antigens on the same section. Positive immunostaining was demonstrated with this procedure with a muscle-specific actin antibody which previously failed to localize antigenic sites by EM. The procedure described yielded staining of high specificity, with minimal background and well-preserved ultrastructure. This re-embedding technique is useful in situations where problems with post-embedding EM immunostaining exist and where correlative LM and EM immunostaining is essential.

摘要

采用胶体金包埋后技术实现了生长激素在大鼠垂体前叶的超微结构定位以及肌肉特异性肌动蛋白在兔动脉平滑肌细胞中的超微结构定位。将塑料切片(2微米)贴于载玻片上,去除塑料,用免疫球蛋白-胶体金颗粒进行免疫染色,重新包埋于环氧树脂中,然后切片用于电子显微镜观察。该方法能够在同一切片上对这些细胞内抗原进行光镜和电镜定位。使用肌肉特异性肌动蛋白抗体通过该方法显示出阳性免疫染色,而该抗体此前未能通过电镜定位抗原位点。所述方法产生的染色具有高特异性,背景极小且超微结构保存良好。这种重新包埋技术在存在包埋后电镜免疫染色问题且相关光镜和电镜免疫染色至关重要的情况下很有用。

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