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KD-Validated NQO2 Recombinant Rabbit mAb

#62309

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using NQO2 antibody (Cat#62309). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with NQO2 antibody (Cat#62309, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using NQO2 antibody (Cat#62309). NQO2 expression in wild type (WT) and NQO2 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with NQO2 antibody (Cat#62309, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with NQO2 antibody (Cat#62309, 1:1,000). Nuclei were stained blue with DAPI; NQO2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Validation of NQO2 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with NQO2 antibody (Cat#62309, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
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Unit price:
$89.00
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  • Gene Symbol:
    NQO2
  • Catalog:
    62309
  • Application:
    WB, FCM, ICC
  • Species Reactivity:
    H, M
Information
Product Name KD-Validated NQO2 Recombinant Rabbit mAb
Aliases NQO2; 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

UniProt Entry: P16083

Application Information

Molecular Weight: Predicted, 26 kDa; observed, 26 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 24GB250

Species Reactivity: Human,mouse

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC)

Immunogen A synthesized peptide derived from human NQO2
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:1,000-1:5,000
Flow Cytometry (FCM): 1:200-1:2,000
Immunocytochemistry (ICC): 1:100-1:1,000
Note This product is for research use only.
Data
  • Western blotting analysis using NQO2 antibody (Cat#62309). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with NQO2 antibody (Cat#62309, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using NQO2 antibody (Cat#62309). NQO2 expression in wild type (WT) and NQO2 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with NQO2 antibody (Cat#62309, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
  • Immunocytochemical staining of HepG2 cells with NQO2 antibody (Cat#62309, 1:1,000). Nuclei were stained blue with DAPI; NQO2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
  • Validation of NQO2 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with NQO2 antibody (Cat#62309, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
Western blotting analysis using NQO2 antibody (Cat#62309). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with NQO2 antibody (Cat#62309, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using NQO2 antibody (Cat#62309). NQO2 expression in wild type (WT) and NQO2 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with NQO2 antibody (Cat#62309, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with NQO2 antibody (Cat#62309, 1:1,000). Nuclei were stained blue with DAPI; NQO2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Validation of NQO2 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with NQO2 antibody (Cat#62309, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
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