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KD-Validated PPP2R5E Recombinant Rabbit mAb

#62517

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using PPP2R5E antibody (Cat#62517). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with PPP2R5E antibody (Cat#62517, 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 PPP2R5E antibody (Cat#62517). PPP2R5E expression in wild type (WT) and PPP2R5E shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with PPP2R5E antibody (Cat#62517, 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 PPP2R5E antibody (Cat#62517, 1:1,000). Nuclei were stained blue with DAPI; PPP2R5E 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 PPP2R5E expression in HepG2 cells using PPP2R5E antibody (Cat#62517, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, PPP2R5E.
Validation of PPP2R5E knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with PPP2R5E antibody (Cat#62517, 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:
    PPP2R5E
  • Catalog:
    62517
  • Application:
    WB, FCM, ICC
  • Species Reactivity:
    H, M, R
Information
Product Name KD-Validated PPP2R5E Recombinant Rabbit mAb
Aliases Protein Phosphatase 2 Regulatory Subunit B'Epsilon; B56epsilon; B56E; Serine/Threonine-Protein Phosphatase 2A 56 KDa Regulatory Subunit Epsilon Isoform; Serine/Threonine Protein Phosphatase 2A, 56 KDa Regulatory Subunit, Epsilon; Protein Phosphatase 2, Regulatory Subunit B (B56), Epsilon Isoform; Protein Phosphatase 2 Regulatory Subunit B', Epsilon; PP2A B Subunit Isoform PR61-Epsilon; PP2A B Subunit Isoform B56-Epsilon; PP2A B Subunit Isoform B'-Epsilon; PP2A B Subunit Isoform R5-Epsilon; PP2A, B Subunit, PR61 Epsilon; PP2A, B Subunit, B56 Epsilon; PP2A, B Subunit, B' Epsilon; PP2A, B Subunit, R5 Epsilon
Background

Gene Name: PPP2R5E

NCBI Gene Entry: 5529

UniProt Entry: Q16537

Application Information

Molecular Weight: Predicted, 55 kDa; observed, 50 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 24GB1215

Species Reactivity: Human,mouse,rat

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

Immunogen A synthesized peptide derived from human PPP2R5E
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 PPP2R5E antibody (Cat#62517). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with PPP2R5E antibody (Cat#62517, 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 PPP2R5E antibody (Cat#62517). PPP2R5E expression in wild type (WT) and PPP2R5E shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with PPP2R5E antibody (Cat#62517, 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 PPP2R5E antibody (Cat#62517, 1:1,000). Nuclei were stained blue with DAPI; PPP2R5E 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 PPP2R5E expression in HepG2 cells using PPP2R5E antibody (Cat#62517, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, PPP2R5E.
  • Validation of PPP2R5E knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with PPP2R5E antibody (Cat#62517, 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 PPP2R5E antibody (Cat#62517). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with PPP2R5E antibody (Cat#62517, 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 PPP2R5E antibody (Cat#62517). PPP2R5E expression in wild type (WT) and PPP2R5E shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with PPP2R5E antibody (Cat#62517, 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 PPP2R5E antibody (Cat#62517, 1:1,000). Nuclei were stained blue with DAPI; PPP2R5E 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 PPP2R5E expression in HepG2 cells using PPP2R5E antibody (Cat#62517, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, PPP2R5E.
Validation of PPP2R5E knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with PPP2R5E antibody (Cat#62517, 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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