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Human NQO2 Knockdown Cell Line (Wb-Validated) #C62309

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RT-qPCR analysis. HeLa cells were infected with NQO2-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
Western blotting analysis. NQO2 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against NQO2 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
  • 基因名:
    NQO2
  • 货号:
    C62309
  • 应用:
  • 物种反应性:
规格:
1 Kit
价格:
询价
Information
Product Name Human NQO2 Knockdown Cell Line (Wb-Validated)
Aliases N-Ribosyldihydronicotinamide:Quinone Dehydrogenase 2; QR2; N-Ribosyldihydronicotinamide:Quinone Reductase 2; NRH:Quinone Oxidoreductase 2; Quinone Reductase 2; NMOR2; DHQV; DIA6; Ribosyldihydronicotinamide Dehydrogenase [Quinone]; NAD(P)H Quinone Dehydrogenase 2; NAD(P)H Menadione Oxidoreductase-1, Dioxin-Inducible-2; NAD(P)H Menadione Oxidoreductase 2, Dioxin-Inducible; Ribosyldihydronicotinamide Dehydrogenase; NAD(P)H Dehydrogenase, Quinone 2; NRH Dehydrogenase [Quinone] 2; EC 1.10.5.1
Background

Gene Name: NQO2

NCBI Gene Entry: 4835

Storage Store at liquid nitrogen for 1 year.
Kit Components 1. Human NQO2 Knockdown Cell Line (Wb-Validated)
2. Wild-type cell line
Parental Cell Line Human cell line supplied by the client
Validation Methods RT-qPCR, Western blotting (WB)
Shipping Shipped on Dry Ice.
Instructions For Use This knockdown cell line should be paired with wild-type cell line for use.
Note This product is for research use only.
Picture
  • RT-qPCR analysis. HeLa cells were infected with NQO2-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
  • Western blotting analysis. NQO2 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against NQO2 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
Citation(0)
RT-qPCR analysis. HeLa cells were infected with NQO2-specific shRNA lentiviral particles, total RNA was extracted from wild-type and knockdown cells, RT-qPCR was performed using gene-specific primers. ∆Ct (CtKD-CtWT) was used to calculate mRNA reduction (%) between wild-type and knockdown cells using the following formula: (1-1/2∆Ct) x 100%.
Western blotting analysis. NQO2 protein expression in wild-type (WT) and shRNA knockdown (KD) HeLa cells was detected using Western blotting. β-Tubulin served as a loading control. The blots were incubated with primary antibodies against NQO2 and β-Tubulin, respectively, followed by incubating with HRP-conjugated goat anti-rabbit secondary antibody. Images were developed using FeQ™ ECL Substrate Kit.
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