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KD-Validated APE1 Recombinant Rabbit mAb

#61682

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using APE1 antibody (Cat#61682). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with APE1 antibody (Cat#61682, 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 APE1 antibody (Cat#61682). APE1 expression in wild type (WT) and APE1 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with APE1 antibody (Cat#61682, 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).
Immunohistochemistry was performed on paraffin-embedded human papillary thyroid carcinoma using APE1 antibody (Cat#61682, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HepG2 cells with APE1 antibody (Cat#61682, 1:1,000). Nuclei were stained blue with DAPI; APE1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Flow cytometric analysis of APE1 expression in HT-1080 cells using APE1 antibody (Cat#61682, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, APE1.
Validation of APE1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with APE1 antibody (Cat#61682, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use.
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Unit price:
$89.00
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1
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  • Gene Symbol:
    APEX1
  • Catalog:
    61682
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, M, R
Information
Product Name KD-Validated APE1 Recombinant Rabbit mAb
Aliases APEX1; Apurinic/Apyrimidinic Endodeoxyribonuclease 1; REF1; HAP1; APEN; APE; APX; REF-1; APE-1; APEX; APEX Nuclease (Multifunctional DNA Repair Enzyme); DNA-(Apurinic Or Apyrimidinic Site) Endonuclease; Apurinic-Apyrimidinic Endonuclease 1; Redox Factor-1; APE1; APEX Nuclease (Multifunctional DNA Repair Enzyme); Deoxyribonuclease (Apurinic Or Apyrimidinic); Apurinic/Apyrimidinic (Antibodyasic) Endonuclease; DNA-(Apurinic Or Apyrimidinic Site) Lyase; AP Endonuclease Class I; AP Endonuclease 1; Protein REF-1; APEX Nuclease; EC 4.2.99.18; EC 3.1.11.2; AP Lyase
Background

Gene Name: APEX1

NCBI Gene Entry: 328

UniProt Entry: P27695

Application Information

Molecular Weight: Predicted, 36 kDa; observed, 36 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB1220

Species Reactivity: Human, mouse, rat

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC), immunohistochemistry-paraffin (IHC-P)

Immunogen A synthesized peptide derived from human APE1
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
Immunohistochemistry-Paraffin (IHC-P): 1:100-1:200
Note This product is for research use only.
Data
  • Western blotting analysis using APE1 antibody (Cat#61682). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with APE1 antibody (Cat#61682, 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 APE1 antibody (Cat#61682). APE1 expression in wild type (WT) and APE1 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with APE1 antibody (Cat#61682, 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).
  • Immunohistochemistry was performed on paraffin-embedded human papillary thyroid carcinoma using APE1 antibody (Cat#61682, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • Immunocytochemical staining of HepG2 cells with APE1 antibody (Cat#61682, 1:1,000). Nuclei were stained blue with DAPI; APE1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
  • Flow cytometric analysis of APE1 expression in HT-1080 cells using APE1 antibody (Cat#61682, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, APE1.
  • Validation of APE1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with APE1 antibody (Cat#61682, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use.
Western blotting analysis using APE1 antibody (Cat#61682). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with APE1 antibody (Cat#61682, 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 APE1 antibody (Cat#61682). APE1 expression in wild type (WT) and APE1 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with APE1 antibody (Cat#61682, 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).
Immunohistochemistry was performed on paraffin-embedded human papillary thyroid carcinoma using APE1 antibody (Cat#61682, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HepG2 cells with APE1 antibody (Cat#61682, 1:1,000). Nuclei were stained blue with DAPI; APE1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Flow cytometric analysis of APE1 expression in HT-1080 cells using APE1 antibody (Cat#61682, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, APE1.
Validation of APE1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with APE1 antibody (Cat#61682, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use.
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