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MSCs are commonly cultured as two-dimensional (2D) monolayer by traditional tissue culture techniques.
Furthermore organs were triturated and cultured for of the presence MAP using standard mycobacterial culture techniques.
MSCs are commonly cultured as a two-dimensional (2D) monolayer using conventional tissue-culture techniques.
New culturing techniques have led to vast improvements.
It has been extensively studied by conventional culture techniques.
Cell culture techniques are essential for studying host pathogen interactions.
Some of these bacteria are not easily detected using standard culturing techniques.
Further genetic research will link sequence diversity with genic factors involved in anther culturing techniques.
Through various breeding and culture techniques, the content of diosgenin could be improved continuously.
Since then human and animal cells culture techniques have improved greatly.
Insufficient culture techniques were assumed to be responsible for the lack of detectable bacteria.
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