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Rt2 profiler pcr array data analysis online software

Manufactured by Qiagen

The RT2 Profiler PCR Array Data Analysis is an online software tool provided by Qiagen. It is designed to analyze data generated from Qiagen's RT2 Profiler PCR Arrays, which are used for the analysis of gene expression profiles.

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5 protocols using rt2 profiler pcr array data analysis online software

1

Real-Time PCR Array for Gene Expression

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RealTimePCR array reactions were performed as previously described [41 (link)–43 (link)]. The extraction of total RNA from the remaining alveolus was performed with the RNeasyFFPE kit (Qiagen Inc, Valencia, CA) according to the manufacturers’ instructions. The integrity of the RNA samples was verified by analyzing 1 mg of total RNA in a 2100Bioanalyzer (Agilent Technologies, Santa Clara, CA) according to the manufacturers’ instructions, and the complementary DNA was synthesized using 3 μg of RNA through a reverse transcription reaction (Superscript III, Invitrogen Corporation, Carlsbad, CA, USA). RealTimePCR array was performed in a Viia7 instrument (LifeTechnologies, Carlsbad, CA) using a custom panel containing targets "Wound Healing" (PAMM-121), "Inflammatory cytokines and receptors"(PAMM-011) and "Osteogenesis" (PAMM-026) (SABiosciences, Frederick, MD) for gene expression profiling. RealTimePCR array data was analyzed by the RT2 profiler PCR Array Data Analysis online software (SABiosciences, Frederick, MD) for normalizing the initial geometric mean of three constitutive genes (GAPDH, ACTB, Hprt1) and subsequently normalized by the control group, and expressed as fold change relative to the control group; as previously described [44 (link), 45 (link)].
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2

Real-Time PCR Analysis of Wound Healing and Inflammatory Cytokines

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A Real Time PCR array was performed as previously described [53 (link)]. Total RNA from SCC-induced tongue lesions; the human cell lines HN12, HN13 and normal oral keratinocyte (NOK); human samples of oral healthy mucosa, healthy skin, inflamed oral mucosa and inflamed skin (used as controls) was obtained with the RNeasyFFPE kit (Qiagen Inc, Valencia, CA, USA) according to the manufacturer's instructions. A Real Time PCR array was performed in a Viia7 instrument (LifeTechnologies, Carlsbad, CA, USA) using the custom panels “Wound Healing” (PAMM-121) and “Inflammatory cytokines and receptors” (PAMM-011) (SABiosciences, Frederick, MD, USA). The data were analysed by the RT2 profiler PCR Array Data Analysis online software (SABiosciences) for normalizing the initial geometric mean of three constitutive genes (GAPDH, ACTB and Hprt1), normalized by the control group and expressed as the fold change relative to the control group.
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3

Profiling TGFβ Signaling Targets

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The array was carried out in duplicate using the Mouse TGFβ Signaling Targets RT2Profiler™ PCR Array (SA Biosciences, PAMM-235Z) according to the manufacturers’ instructions. Cells were plated and exposed to TGFβ2 and/or bFGF for 48 hours. Total RNA was purified with an RNeasy Mini Kit (Qiagen) and cDNA synthesis was performed with an iScript cDNA Synthesis Kit (Bio-Rad). ABI 7900HT Quantitative PCR System was used for the qPCR array and the data were analyzed with SA Biosciences’ RT2 Profiler™ PCR Array Data Analysis Online Software.
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4

Real-Time PCR Analysis of Wound Healing, Inflammation, and Osteogenesis

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Real Time PCR array reactions were performed as previously described (25 (link), 47 (link)). In short, extraction of total RNA from the remaining alveolus was performed with the RNeasy Plus kit (Qiagen Inc, Valencia, CA) according to the manufacturer’s instructions. The integrity of the RNA samples was verified by analyzing 1 µl of the total RNA in a 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA) according to the manufacturer’s instructions, and the complementary DNA (cDNA) was synthesized using 1 mg of RNA through a reverse transcription reaction QuantiTect Rev Transcription kit (Qiagen Inc, Valencia, CA). Real Time PCR array was performed in a Viia7 instrument (Thermo Fisher Scientific, Carlsbad, CA) using a custom panel containing targets “Wound Healing” (PAMM-121), “Inflammatory cytokines and receptors” (PAMM-011), and “Osteogenesis” (PAMM-026) (SA Biosciences, Frederick, MD) for gene expression profiling. Real Time PCR array data were analyzed by the RT2 profiler PCR Array Data Analysis online software (SA Biosciences, Frederick, MD) for normalizing the initial geometric mean of three constitutive genes (GAPDH, ACTB, Hprt1) and subsequently normalized by the control group, and expressed as fold change relative to the control group.
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5

Quantitative Real-Time PCR Analysis of Wound Healing and Inflammatory Responses

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Real-Time PCR array reactions were performed as previously described.4 (link)
The extraction of total RNA from the remaining alveolus was performed with the RNeasy FFPE kit (Qiagen Inc., Valencia, CA) according to the manufacturers’ instructions. The integrity of the RNA samples was verified by analyzing 1mg of total RNA in a 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA) according to the manufacturers’ instructions, and the complementary DNA was synthesized using 3μg of RNA by a reverse transcription reaction (Superscript III, Invitrogen Corporation, Carlsbad, CA). Real-Time PCR array was performed in a ViiA7 instrument (LifeTechnologies, Carlsbad, CA) using a custom panel containing the targets “Wound Healing” (PAMM-121), “Inflammatory cytokines and receptors” (PAMM-011), and “Osteogenesis” (PAMM-026) (SABiosciences, Frederick, MD), as well as for NOS isoforms (iNOS, nNOS, and eNOS), used for gene expression profiling. Real-Time PCR array data was analyzed by the RT2 profiler PCR Array Data Analysis online software (SABiosciences, Frederick, MD) to normalize the initial geometric mean of three constitutive genes (GAPDH, ACTB, Hprt1) and then normalized by the control group (comprising an additional independent group of mice, not subjected to any surgical procedure), and expressed as fold change regarding the control group, as previously described.4 (link)
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