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首页> 外文期刊>Journal of Immunological Methods >A high capacity in vitro assay for measuring the cytoadherence of Plasmodium falciparum-infected erythrocytes.
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A high capacity in vitro assay for measuring the cytoadherence of Plasmodium falciparum-infected erythrocytes.

机译:一种用于测量恶性疟原虫感染的红细胞的细胞粘附性的体外检测方法。

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摘要

A simple, efficient, sensitive, reproducible and high throughput assay for measuring the cytoadhesion of Plasmodium falciparum-infected red blood cells (human malaria) is described. The assay format uses 96-well microplates, with the number of P. falciparum parasitized erythrocytes bound determined by measuring Plasmodium specific lactic dehydrogenase activity colorimetrically (absorbance at 655 nm) using the 3-acetylpyridine analog of nicotinamide adenine dinucleotide, nitro blue tetrazolium and diaphorase. The results of the described microplate assay were found to be comparable to those using microscopic analysis but much less time consuming.
机译:描述了一种简单,有效,灵敏,可重现和高通量的测定方法,用于测量恶性疟原虫感染的红细胞(人疟疾)的细胞粘附。该测定形式使用96孔微孔板,结合的恶性疟原虫寄生的红细胞数量是通过使用烟酰胺腺嘌呤二核苷酸,硝基蓝四唑和黄递质酶的3-乙酰吡啶类似物比色法测定疟原虫特异性乳酸脱氢酶活性(在655 nm处的吸光度)来确定的。发现所描述的微孔板测定法的结果与使用显微镜分析的结果相当,但是耗时少得多。

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