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培养细胞和啮齿动物脑区的谷胱甘肽含量:一种特异性荧光测定法。

Glutathione content of cultured cells and rodent brain regions: a specific fluorometric assay.

作者信息

Mokrasch L C, Teschke E J

出版信息

Anal Biochem. 1984 Aug 1;140(2):506-9. doi: 10.1016/0003-2697(84)90201-x.

Abstract

The glutathione contents of cultured cells and rodent brain were determined by a fluorometric procedure which eliminates the interference of endogenous histidine-containing compounds. Cultured neonatal rat and hamster astrocytes, human dermal fibroblasts, and mouse and rat brain regions were assayed. o-Phthalaldehyde forms a fluorescent complex with glutathione, oxidized glutathione, and histidyl compounds in the absence of added thiol. The reaction of histidyl compounds can be abolished by the addition of formaldehyde to the reaction mixtures. A 10-pmol quantity of glutathione can be measured in dilute formic acid extracts of milligram quantities of tissue.

摘要

采用一种荧光法测定培养细胞和啮齿动物脑内的谷胱甘肽含量,该方法可消除内源性含组氨酸化合物的干扰。对培养的新生大鼠和仓鼠星形胶质细胞、人皮肤成纤维细胞以及小鼠和大鼠的脑区进行了检测。在不添加硫醇的情况下,邻苯二甲醛与谷胱甘肽、氧化型谷胱甘肽和组氨酸化合物形成荧光复合物。向反应混合物中加入甲醛可消除组氨酸化合物的反应。在毫克量组织的稀甲酸提取物中可检测到10皮摩尔量的谷胱甘肽。

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