Simulation and experimental study of temprature lag time for Polymerase Chain Reaction instrument

2010 ◽  
Author(s):  
Jing Huang ◽  
Zhangwei Chen ◽  
Yinghao Yao ◽  
Juanrong Liu
Keyword(s):  
Experimental Study ◽  
Polymerase Chain Reaction ◽  
Lag Time ◽  
Chain Reaction ◽  
Polymerase Chain Reaction Instrument ◽  
Polymerase Chain

A Reusable Flow-Through Polymerase Chain Reaction Instrument for the Continuous Monitoring of Infectious Biological Agents

2003 ◽  
Vol 75 (14) ◽  
pp. 3446-3450 ◽  
Author(s):  
Phillip Belgrader ◽  
Christopher J. Elkin ◽  
Steven B. Brown ◽  
Shanavaz N. Nasarabadi ◽  
Richard G. Langlois ◽  
...  
Keyword(s):  
Polymerase Chain Reaction ◽  
Continuous Monitoring ◽  
Biological Agents ◽  
Chain Reaction ◽  
Polymerase Chain Reaction Instrument ◽  
Flow Through ◽  
Polymerase Chain

scholarly journals Multicenter International Work Flow Study of an Automated Polymerase Chain Reaction Instrument

1998 ◽  
Vol 44 (8) ◽  
pp. 1737-1739 ◽  
Author(s):  
Paul E Klapper ◽  
Donald L Jungkind ◽  
Thomas Fenner ◽  
Roberto Antinozzi ◽  
Jurjen Schirm ◽  
...  
Keyword(s):  
Polymerase Chain Reaction ◽  
Work Flow ◽  
Chain Reaction ◽  
International Work ◽  
Polymerase Chain Reaction Instrument ◽  
Polymerase Chain ◽  
Flow Study

High performance Nanogold™-in situ hybridzation and its use in the detection of hybridized and PCR-amplified microscopical preparations

1996 ◽  
Vol 54 ◽  
pp. 896-897
Author(s):  
G. W. Hacker ◽  
I. Zehbe ◽  
J. Hainfeld ◽  
A.-H. Graf ◽  
C. Hauser-Kronberger ◽  
...  
Keyword(s):  
Polymerase Chain Reaction ◽  
Messenger Rna ◽  
High Performance ◽  
Detection System ◽  
Direct Methods ◽  
Genetic Alterations ◽  
Chain Reaction ◽  
Protein Encoding ◽  
Polymerase Chain

In situ hybridization (ISH) with biotin-labeled probes is increasingly used in histology, histopathology and molecular biology, to detect genetic nucleic acid sequences of interest, such as viruses, genetic alterations and peptide-/protein-encoding messenger RNA (mRNA). In situ polymerase chain reaction (PCR) (PCR in situ hybridization = PISH) and the new in situ self-sustained sequence replication-based amplification (3SR) method even allow the detection of single copies of DNA or RNA in cytological and histological material. However, there is a number of considerable problems with the in situ PCR methods available today: False positives due to mis-priming of DNA breakdown products contained in several types of cells causing non-specific incorporation of label in direct methods, and re-diffusion artefacts of amplicons into previously negative cells have been observed. To avoid these problems, super-sensitive ISH procedures can be used, and it is well known that the sensitivity and outcome of these methods partially depend on the detection system used.

1504: Molecular Diagnosis and Staging of Prostate Cancer Using Clusterin in Real Time Reverse Transcription Polymerase Chain Reaction (RT-PCR)

2006 ◽  
Vol 175 (4S) ◽  
pp. 485-486
Author(s):  
Sabarinath B. Nair ◽  
Christodoulos Pipinikas ◽  
Roger Kirby ◽  
Nick Carter ◽  
Christiane Fenske
Keyword(s):  
Prostate Cancer ◽  
Polymerase Chain Reaction ◽  
Real Time ◽  
Molecular Diagnosis ◽  
Reverse Transcription ◽  
Rt Pcr ◽  
Chain Reaction ◽  
Polymerase Chain
Sign in / Sign up

Export Citation Format

Share Document