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KO-Validated Phospho-Smad3 (S423 + S425) Recombinant Rabbit mAb

#71222

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Recombinant Antibody
Knockout Validated
Western blotting analysis using phospho-Smad3 (S423 + S425) antibody (Cat#71222). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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 phospho-Smad3 (S423 + S425) antibody (Cat#71222). Phospho-Smad3 (S423 + S425) expression in wild-type (WT) and SMAD3 knockout (KO) HSHC cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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).
Immunohistochemistry was performed on paraffin-embedded human gastric carcinoma using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
Immunohistochemistry was performed on paraffin-embedded mouse kidney using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
Immunohistochemistry was performed on paraffin-embedded mouse liver using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
Immunohistochemistry was performed on paraffin-embedded mouse lung using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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 HAP-1 cells with Phospho-Smad3 (S423 + S425) antibody (Cat#71222, 1:1,000). Nuclei were stained blue with DAPI; Phospho-Smad3 (S423 + S425) 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 Phospho-Smad3 (S423 + S425) expression in HAP-1 cells using Phospho-Smad3 (S423 + S425) antibody (Cat#71222, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Phospho-Smad3 (S423 + S425).
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  • Gene Symbol:
    SMAD3
  • Catalog:
    71222
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, M, R
Information
Product Name KO-Validated Phospho-Smad3 (S423 + S425) Recombinant Rabbit mAb
Aliases SMAD3; SMAD Family Member 3; JV15-2; HsT17436; MADH3; Mothers Against Decapentaplegic Homolog 3; Mothers Against DPP Homolog 3;
MAD Homolog 3; HMAD-3; HSMAD3; Mad3; MAD, Mothers Against Decapentaplegic Homolog 3 (Drosophila); SMAD, Mothers Against DPP Homolog 3 (Drosophila); MAD, Mothers Against Decapentaplegic Homolog 3; SMAD, Mothers Against DPP Homolog 3; SMA- And MAD-Related Protein 3; Mad Protein Homolog; Mad Homolog JV15-2; HSPC193; SMAD 3; LDS1C; Smad3; LDS3
Background

Gene Name: SMAD3

NCBI Gene Entry: 4088

UniProt Entry: P84022

Application Information

Molecular Weight: Predicted, 61 kDa; observed, 60 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 25GB3215

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 Phospho-Smad3 (S423 + S425)
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 phospho-Smad3 (S423 + S425) antibody (Cat#71222). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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 phospho-Smad3 (S423 + S425) antibody (Cat#71222). Phospho-Smad3 (S423 + S425) expression in wild-type (WT) and SMAD3 knockout (KO) HSHC cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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).
  • Immunohistochemistry was performed on paraffin-embedded human gastric carcinoma using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
  • Immunohistochemistry was performed on paraffin-embedded mouse kidney using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
  • Immunohistochemistry was performed on paraffin-embedded mouse liver using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
  • Immunohistochemistry was performed on paraffin-embedded mouse lung using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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 HAP-1 cells with Phospho-Smad3 (S423 + S425) antibody (Cat#71222, 1:1,000). Nuclei were stained blue with DAPI; Phospho-Smad3 (S423 + S425) 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 Phospho-Smad3 (S423 + S425) expression in HAP-1 cells using Phospho-Smad3 (S423 + S425) antibody (Cat#71222, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Phospho-Smad3 (S423 + S425).
Western blotting analysis using phospho-Smad3 (S423 + S425) antibody (Cat#71222). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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 phospho-Smad3 (S423 + S425) antibody (Cat#71222). Phospho-Smad3 (S423 + S425) expression in wild-type (WT) and SMAD3 knockout (KO) HSHC cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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).
Immunohistochemistry was performed on paraffin-embedded human gastric carcinoma using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
Immunohistochemistry was performed on paraffin-embedded mouse kidney using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
Immunohistochemistry was performed on paraffin-embedded mouse liver using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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.
Immunohistochemistry was performed on paraffin-embedded mouse lung using phospho-Smad3 (S423 + S425) antibody (Cat#71222, 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 HAP-1 cells with Phospho-Smad3 (S423 + S425) antibody (Cat#71222, 1:1,000). Nuclei were stained blue with DAPI; Phospho-Smad3 (S423 + S425) 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 Phospho-Smad3 (S423 + S425) expression in HAP-1 cells using Phospho-Smad3 (S423 + S425) antibody (Cat#71222, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Phospho-Smad3 (S423 + S425).
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