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Titlebook: Basic Cell Culture Protocols; Cheryl D. Helgason,Cindy L. Miller Book 20053rd edition Humana Press 2005 DNA.Macrophages.cell.cell culture.

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51#
發(fā)表于 2025-3-30 11:31:48 | 只看該作者
Isolation, Purification, and Cultivation of Murine and Human Keratinocytes, chapter describes the methodology required to isolate, purify, and cultivate keratinocytes to produce both monolayer and stratified cultures. The methodologies for producing cultures of keratinocytes obtained from rat skin and from human skin are described.
52#
發(fā)表于 2025-3-30 15:34:18 | 只看該作者
53#
發(fā)表于 2025-3-30 20:37:03 | 只看該作者
54#
發(fā)表于 2025-3-30 23:56:51 | 只看該作者
55#
發(fā)表于 2025-3-31 03:30:05 | 只看該作者
56#
發(fā)表于 2025-3-31 07:36:52 | 只看該作者
Book 20053rd editionsolation of side-population cells, and scalable production of ES-derived cells) and detail quality control methods for cell lines (detection and elimination of mycoplasma, DNA fingerprinting, and cytogenetic analysis).
57#
發(fā)表于 2025-3-31 09:12:15 | 只看該作者
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發(fā)表于 2025-3-31 16:42:39 | 只看該作者
Detection of Mycoplasma Contaminations,oplasma contamination is an important part of mycoplasma control and should be an established method in every cell culture laboratory. New cell lines as well as cell lines in continuous culture must be tested in regular intervals. The polymerase chain reaction (PCR) methodology offers a fast and sen
59#
發(fā)表于 2025-3-31 18:52:46 | 只看該作者
Eradication of Mycoplasma Contaminations,active substances used in human medicine. The elimination of mycoplasma contaminations in cell cultures has become a practical alternative to discarding and re-establishing important or irreplaceable cell lines. Different quinolones, tetracyclins, and macrolides shown to have strong antimycoplasma p
60#
發(fā)表于 2025-3-31 23:41:35 | 只看該作者
Authentication of Scientific Human Cell Lines,es. In this regard, it is crucial that the cells faithfully correspond to the purported objects of study. A number of recent publications have shown an unacceptable level of cell lines to be false, in part as a result of the nonavailability of a simple and easy DNA profiling technique. We have valid
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