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用于电子显微镜检查的组织制备过程中糖蛋白的提取。

Extraction of glycoproteins during tissue preparation for electron microscopy.

作者信息

Sturgess J M, Mitranic M M, Moscarello M A

出版信息

J Microsc. 1978 Sep;114(1):101-5. doi: 10.1111/j.1365-2818.1978.tb00120.x.

Abstract

The extraction of glycoproteins labelled with 3H or 14C precursors: fucose and glucosamine, has been compared during processing of rat liver for transmission electron microscopy. Using 14C labelled fucose, approximately 6% of labelled macromolecules were extracted during processing including 3% during glutaraldehyde fixation, 1% during post-fixation and 2% during dehydration. Greater extraction (8%) occurs with glucosamine as a precursor, which may be attributed to hydrolysis of the more labile sialic acid residues of the glycoprotein molecules. Tritium labelled glycoproteins were more susceptible to extraction than 14C-labelled glycoproteins. The extraction of 3H-labelled glycoproteins as measured by liquid scintillation counting may prove difficult to interpret owing to the quenching from processing solutions.

摘要

在对大鼠肝脏进行透射电子显微镜检查的过程中,对用³H或¹⁴C前体(岩藻糖和氨基葡萄糖)标记的糖蛋白的提取情况进行了比较。使用¹⁴C标记的岩藻糖时,在处理过程中约6%的标记大分子被提取出来,其中包括在戊二醛固定期间提取3%,后固定期间提取1%,脱水期间提取2%。以氨基葡萄糖作为前体时提取率更高(8%),这可能归因于糖蛋白分子中更不稳定的唾液酸残基的水解。³H标记的糖蛋白比¹⁴C标记的糖蛋白更容易被提取。由于处理溶液的淬灭作用,通过液体闪烁计数法测量³H标记糖蛋白的提取情况可能难以解释。

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