2010
DOI: 10.4014/jmb.1004.04035
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Quantitative Detection of Residual E. coli Host Cell DNA by Real-Time PCR

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Cited by 26 publications
(13 citation statements)
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“…They may potentially cause allergic reactions (proteins) or even genetic disruption (DNA) resulting in tumours (Lee et al . ). Therefore, a large number of reports on process development have chosen HCP and host cell DNA clearance as a benchmark to demonstrate a well‐controlled bioprocess.…”
Section: Discussionmentioning
confidence: 97%
“…They may potentially cause allergic reactions (proteins) or even genetic disruption (DNA) resulting in tumours (Lee et al . ). Therefore, a large number of reports on process development have chosen HCP and host cell DNA clearance as a benchmark to demonstrate a well‐controlled bioprocess.…”
Section: Discussionmentioning
confidence: 97%
“…Similar to the previous work, the primers used in the MELGA technique displayed high specificity for the leukemic K562 cell line ( BCR/ABL expression). The detection limit for this technique is <1 fg/ml of RNA in the K562 cell line, which is lower than RQ‐PCR , conventional PCR , and ELISA (i.e., picogram, nanogram, and nanogram, respectively). At <1 fg/ml of total RNA, the OD was slightly increased.…”
Section: Discussionmentioning
confidence: 87%
“…Other parameters such as cost, experienced personnel, interpretability, validity of results, and applicability are among the factors that influence the approval of final results. Therefore, the functional characteristics of each method used should be evaluated [30][31][32][33]. Even though easy to set up conventional radiolabeled hybridization based methods have low precision due to the instability and short life-span of radio-isotopes [19].…”
Section: Discussionmentioning
confidence: 99%