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Adv Exp Med Biol. 2018;1119:151-168. doi: 10.1007/5584_2018_277.

Selection of Suitable Reference Genes for Quantitative Real-Time PCR Normalization in Human Stem Cell Research.

Author information

1
Tissue Engineering, Biomaterials and Nanobiotechnology Laboratory, Ankara University Faculty of Science, and Ankara University Stem Cell Institute, Ankara, Turkey.
2
Tissue Engineering, Biomaterials and Nanobiotechnology Laboratory, Ankara University Faculty of Science, and Ankara University Stem Cell Institute, Ankara, Turkey. elcin@ankara.edu.tr.
3
Biovalda Health Technologies, Inc., Ankara, Turkey. elcin@ankara.edu.tr.

Abstract

Quantitative real-time polymerase chain reaction (qRT-PCR) is a widely utilized method for evaluating the gene expressions in stem cell research. This method enables researchers to obtain fast and precise results, but the accuracy of the data depends on certain factors, such as those associated with biological sample preparation and PCR efficiency. In order to achieve accurate and reliable results, it is of utmost importance to designate the reference genes, the expressions of which are suitable to all kinds of experimental conditions. Hence it is vital to normalize the qRT-PCR data by using the reference genes. In recent years, it has been found that the expression levels of reference genes widely used in stem cell research present a substantial amount of variation and are not necessarily suitable for normalization. This chapter at hand stresses the significance of selecting suitable reference genes from the point view of human stem cell research.

KEYWORDS:

Housekeeping genes; Human; Reference genes; Stem cells; qRT-PCR; qRT-PCR normalization

PMID:
30267307
DOI:
10.1007/5584_2018_277
[Indexed for MEDLINE]

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