2015
DOI: 10.1590/s1516-8913201400130
|View full text |Cite
|
Sign up to set email alerts
|

Quality Control of Biotechnological Inputs DetectingMycoplasma

Abstract: The aim of this work was to study the Polymerase Chain Reaction (PCR) as a tool of quality control of bovine sera and cellular cultures used in the biotechnological industry. A total of 46 samples of bovine sera derived from two slaughterhouses and 33 samples of BHK21 cells derived from two biotechnological industries were evaluated using the primers GPO-3 (sense) and MGSO (antisense). The

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2020
2020
2021
2021

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 20 publications
0
1
0
Order By: Relevance
“…The human non-small cell lung cell line, H1299, pCB6+ vector, WT p53 and p53 H175 pCB6+ plasmids were kindly provided by Professor Karen Vousden (The Beatson Institute for Cancer Research, UK). Mycoplasma contamination was absent in all cell lines (28). Recombinant pCB6+ based plasmids carrying full-the length WT TP53 K100 and del TP53 M213 were constructed with cDNA following the RT-PCR amplification of RNA from KKU-100 and KKU-M213 cells.…”
Section: Methodsmentioning
confidence: 99%
“…The human non-small cell lung cell line, H1299, pCB6+ vector, WT p53 and p53 H175 pCB6+ plasmids were kindly provided by Professor Karen Vousden (The Beatson Institute for Cancer Research, UK). Mycoplasma contamination was absent in all cell lines (28). Recombinant pCB6+ based plasmids carrying full-the length WT TP53 K100 and del TP53 M213 were constructed with cDNA following the RT-PCR amplification of RNA from KKU-100 and KKU-M213 cells.…”
Section: Methodsmentioning
confidence: 99%