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NQO-1 is a lab equipment product designed for the detection and measurement of the enzyme NAD(P)H:quinone oxidoreductase 1 (NQO1). NQO1 is an enzyme involved in cellular redox processes and plays a role in detoxification. The NQO-1 product provides a tool for researchers to study the activity and expression of this enzyme in various biological samples and experimental systems.

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5 protocols using nqo 1

1

Quantifying NQO-1, Nrf2 Expression

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Real-time PCR were performed as previously described [9 (link)] using primers for NQO-1, Nrf2, and actin (Life Technologies, Grand Island, NY).
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2

Quantifying Transcriptional Regulators in Skin

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The primers and probes (TaqMan® Gene Expression Assays) used to measure the mRNA levels for Keap1, Nrf1, Nrf3, NQO1, GSTP, GCLC, HMOX-1, IL-6, IL-1β, and COX2 were from Life Technologies. Total RNA was extracted from mouse skin using RNeasy Fibrous Tissue Kit (Qiagen Ltd.). Omniscript RT Kit (Qiagen Ltd.) was then used to reverse-transcribe 500 ng of total RNA into cDNA. Real-time PCR was carried out on Perkin Elmer/Applied Biosystems Prism Model 7700 Sequence Detector instrument. The TaqMan data for the mRNA species were normalized using β-actin (mouse ACTB, 4352933E) as an internal control.
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3

qPCR for Ho1 and Nqo1 Gene Expression

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qPCR was performed as described in our previous studies [39 (link), 40 (link)]. Primers for Ho1 and Nqo1 were purchased from Life Technologies (Grand Island, NY, USA).
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4

Comprehensive Gene Expression Analysis

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Total RNA was extracted from tissues and cells using the Trizol method. The cDNA was synthesized using a high-capacity cDNA reverse transcription kit. qRT-PCR was performed on the ABI PRISM 7,500 Sequence Detection System. Primers for NNMT, TNF-α, IL-6, IL-1, TGF-β, Nrf2, heme oxygenase-1 (HO-1), glutamate-cysteine ligase (GCLC), and NADPH quinineoxidoreductase-1 (NQO-1), type 1 collagen, connective tissue growth factor (CTGF), matrix metallopeptidase 9 (MMP-9), α-myosin heavy chain (α-MyHC), brain natriuretic peptide (BNP), and β-actin were purchased from Life Technologies. The mouse housekeeping gene β-actin was used as an internal control. Relative mRNA expression levels were normalized to β-actin. The primer sequences are provided in Supplementary Table 1.
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5

Quantitative Real-Time PCR Analysis

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Quantitative real-time PCR was performed as previously described (Wang et al. 2009 (link), Wu et al. 2014) (link). Primers for collagen 4 (Col4), Fn, Gapdh, Nqo1, intercellular adhesion molecule 1 (Icam-1), Ho1, iNos, Keap1, Nrf2 and Vcam-1 were all purchased from Life Technologies.
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