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通过将微孔酶联免疫吸附测定(Microelisa)孔溶解在闪烁液中来直接计数氚。

Direct counting of tritium by dissolving Microelisa wells in scintillation fluid.

作者信息

Tandon A K, Chamness G C, McGuire W L

出版信息

J Immunol Methods. 1986 Sep 27;92(2):281-3. doi: 10.1016/0022-1759(86)90176-6.

Abstract

Radioassays with low-energy beta-emitting nuclides (e.g., 3H, 14C, 35S) in 96-well plastic plates are tedious and frequently inaccurate because of the necessity of quantitatively removing and transferring the contents of each well to scintillation fluid. We therefore investigated the possibility of counting these nuclides by directly placing the entire break-apart well (Microelisa) along with the sample into one of four scintillation counting fluids: toluene-PPO-POPOP with or without Protosol, ACSR, and EcoLite. Although some of these scintillation fluids fully dissolved the plastic wells and other did not, we found that the presence of the wells did not appreciably interfere with the efficiency of tritium counting. This technique saves considerable time and reduces possible errors in liquid scintillation counting of samples from plastic microtitration plates.

摘要

在96孔塑料板中使用低能β发射核素(如³H、¹⁴C、³⁵S)进行放射性测定既繁琐又常常不准确,因为需要定量去除并将每个孔中的内容物转移到闪烁液中。因此,我们研究了将整个破碎的孔(微量酶标板)连同样品一起直接放入四种闪烁计数液之一中来计数这些核素的可能性:含或不含Protosol的甲苯-PPO-POPOP、ACSR和EcoLite。尽管其中一些闪烁液能完全溶解塑料孔,而另一些则不能,但我们发现孔的存在并未明显干扰氚计数的效率。该技术节省了大量时间,并减少了塑料微量滴定板样品液体闪烁计数中可能出现的误差。

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