Albers A C, Fletcher R D
Appl Environ Microbiol. 1982 Apr;43(4):958-60. doi: 10.1128/aem.43.4.958-960.1982.
A rapid, simple, and inexpensive method for quantitation of viable mycoplasmas is described. Serial dilutions were made in sterile microtiter plates with standard microtiter equipment. The results were multiplied by a factor of 2.38 to obtain colony-forming units comparable to those obtained with the laborious glass pipette-tube dilution method.
本文描述了一种快速、简单且廉价的定量活支原体的方法。使用标准微量滴定设备在无菌微量滴定板中进行系列稀释。结果乘以2.38的系数,以获得与使用繁琐的玻璃吸管-试管稀释法所获得的相当的菌落形成单位。