Semiquantitative reverse transcription-polymerase chain reaction with the Agilent 2100 Bioanalyzer

被引:0
作者
Gottwald, E
Müller, O
Polten, A
机构
[1] Forschungszentrum Karlsruhe, Inst Med Tech & Biophys, D-76021 Karlsruhe, Germany
[2] Agilent Technol Deutschland GmbH, Waldbronn, Germany
关键词
primer-dropping; LabChip; bioanalyzer; capillary electrophoresis; heat shock protein 72;
D O I
10.1002/1522-2683(200110)22:18<4016::AID-ELPS4016>3.0.CO;2-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have applied a method to monitor mRNA expression in a semiquantitative fashion on the Agilent 2100 Bioanalyzer. The method was originally described in 1994 by Wong, et al. and referred to as the ,,primer-dropping" method. This polymerase chain. reaction (PCR) technique uses multiple sets of primer pairs in a coamplification reaction that amplifies the target of interest within a predetermined range specific for each target. Separation, detection and quantification of PCR products were accomplished using the Agilent 2100 Bioanalyzer in conjunction with the DNA 500 and the DNA 1000 Lab-Chip kits for the detection of DNA fragments with a maximum size of 500 and 1000 bp, respectively. Using primers specific for the inducible form of hsp72 and primers for glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as an internal standard we were. able to rapidly monitor and quantify inducible hsp72-mRNA expression.
引用
收藏
页码:4016 / 4022
页数:7
相关论文
共 18 条
[1]   ABSOLUTE MESSENGER-RNA QUANTIFICATION USING THE POLYMERASE CHAIN-REACTION (PCR) - A NOVEL-APPROACH BY A PCR AIDED TRANSCRIPT TITRATION ASSAY (PATTY) [J].
BECKERANDRE, M ;
HAHLBROCK, K .
NUCLEIC ACIDS RESEARCH, 1989, 17 (22) :9437-9446
[2]   VARIOUS RAT ADULT TISSUES EXPRESS ONLY ONE MAJOR MESSENGER-RNA SPECIES FROM THE GLYCERALDEHYDE-3-PHOSPHATE-DEHYDROGENASE MULTIGENIC FAMILY [J].
FORT, P ;
MARTY, L ;
PIECHACZYK, M ;
ELSABROUTY, S ;
DANI, C ;
JEANTEUR, P ;
BLANCHARD, JM .
NUCLEIC ACIDS RESEARCH, 1985, 13 (05) :1431-1442
[3]  
GIEGERICH R, 1996, P 4 INT C INT SYST M, P68
[4]  
GILILAND G, 1990, P NATL ACAD SCI USA, V87, P2725
[5]   KINETIC PCR ANALYSIS - REAL-TIME MONITORING OF DNA AMPLIFICATION REACTIONS [J].
HIGUCHI, R ;
FOCKLER, C ;
DOLLINGER, G ;
WATSON, R .
BIO-TECHNOLOGY, 1993, 11 (09) :1026-1030
[6]  
HORIKOSHI T, 1992, CANCER RES, V52, P108
[7]  
LIVAK KJ, 1995, PCR METH APPL, V4, P357
[8]   QUANTITATION OF CYTOKINE MESSENGER-RNA LEVELS UTILIZING THE REVERSE TRANSCRIPTASE-POLYMERASE CHAIN-REACTION FOLLOWING PRIMARY ANTIGEN-SPECIFIC SENSITIZATION INVIVO .1. VERIFICATION OF LINEARITY, REPRODUCIBILITY AND SPECIFICITY [J].
MOHLER, KM ;
BUTLER, LD .
MOLECULAR IMMUNOLOGY, 1991, 28 (4-5) :437-447
[9]  
Mueller O, 2000, ELECTROPHORESIS, V21, P128, DOI 10.1002/(SICI)1522-2683(20000101)21:1<128::AID-ELPS128>3.0.CO
[10]  
2-M