Quantitative PCR

EP Esmee K. van der Ploeg
KG Korneliusz Golebski
MN Menno van Nimwegen
JF Joannah R. Fergusson
BH Balthasar A. Heesters
IM Itziar Martinez-Gonzalez
CK Chantal M. A. Kradolfer
ST Sophie van Tol
BS Brendon P. Scicluna
MB Marjolein J. W. de Bruijn
GB Geertje M. de Boer
GT Gerdien A. Tramper-Stranders
GB Gert-Jan Braunstahl
WI Wilfred F. J. van IJcken
AN A. Paul Nagtegaal
CD Cornelis M. van Drunen
WF Wytske J. Fokkens
DH Danny Huylebroeck
HS Hergen Spits
RH Rudi W. Hendriks
RS Ralph Stadhouders
SB Suzanne M. Bal
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RNA was isolated from sorted or cultured ILC2s using the RNeasy Micro Kit (Qiagen) according to the manufacturer’s instructions. RNA was synthesized into complementary DNA using RevertAid H Minus Reverse Transcriptase and random hexamer primers in the presence of RiboLock RNase inhibitor (Thermo Fisher Scientific). For quantitative reverse transcription polymerase chain reaction (qRT-PCR) reactions, probes from the Universal ProbeLibrary Set (Roche Applied Science) and TaqMan Universal Master Mix were used (Applied Biosystems, Foster City, CA, USA). qRT-PCRs were performed using the Prism 7300 Sequence Detection System (Applied Biosystems).

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