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Comparison between Real-Time PCR and Agarose Gel Electrophoresis for DNA Quantification / 대한진단검사의학회지
The Korean Journal of Laboratory Medicine ; : 217-222, 2006.
Article in Korean | WPRIM | ID: wpr-30977
ABSTRACT

BACKGROUND:

Real-time polymerase chain reaction (PCR) is generally regarded as a very accurate and time-saving method, but it is expensive to run. We evaluated the reliability of an inexpensive and a researcher-friendly gel electrophoresis-based PCR method for the quantification of mRNA, and the results were compared with those obtained by real-time PCR.

METHODS:

We compared the results of relative quantification for MMP-1 measured by real-time PCR and by ethidium bromide stained-agarose gel electrophoresis after end-point PCR.

RESULTS:

There was significant but very weak correlation between real-time PCR and end-point PCR for relative quantification of MMP-1 (r=0.16, P<0.01).

CONCLUSIONS:

Our results suggest that the use of the gel electrophoresis-based end-point PCR is inappropriate for quantifying mRNA. Therefore, in order to confirm the result of relative quantification by end-point PCR, the newly established real-time PCR method or northern hybridization should be applied.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Sepharose / DNA / RNA, Messenger / Polymerase Chain Reaction / Electrophoresis / Electrophoresis, Agar Gel / Ethidium / Real-Time Polymerase Chain Reaction Language: Korean Journal: The Korean Journal of Laboratory Medicine Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Sepharose / DNA / RNA, Messenger / Polymerase Chain Reaction / Electrophoresis / Electrophoresis, Agar Gel / Ethidium / Real-Time Polymerase Chain Reaction Language: Korean Journal: The Korean Journal of Laboratory Medicine Year: 2006 Type: Article