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Anti-Vimentin Mouse Monoclonal Antibody #3471

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Flow cytometric analysis of vimentin expression in HepG2 cells using anti-vimentin antibody (Cat#3471, 1:2,000). Green, isotype control; red, vimentin.
Immunocytochemical staining of HepG2 cells with anti-Vimentin antibody (Cat#3471, 1:1,000) . Nuclei were stained blue with DAPI; Vimentin was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and Smart Gain:Medium. Scale bar, 20 μm.
Immunohistochemistry was performed on paraffin-embedded human endometrial carcinoma using anti-vimentin antibody (Cat#3471, 1:100). 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.
Western blotting analysis using anti-vimentin antibody (Cat#3471). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-vimentin antibody (Cat#3471, 1:5,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit(Cat#716).
  • 基因名:
    VIM
  • 货号:
    3471
  • 应用:
    WB, FCM, IC, IHC
  • 物种反应性:
    H
规格:
20 μL,50 μL,100 μL
价格:
¥ 620.00,¥ 1,200.00,¥ 2,200.00
Information
Product Name Anti-Vimentin Mouse Monoclonal Antibody
Aliases VIM; Vimentin; Epididymis Secretory Sperm Binding Protein
Background

Gene Name: VIM

NCBI Gene Entry: 7431

UniProt Entry: P08670

Application Information

Molecular Weight: Predicted, 54 kDa; observed, 54 kDa

Clonality: Mouse monoclonal antibody

Clone ID: 24GB5785

Species Reactivity: Human

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (IC), immunohistochemistry (IHC)

Immunogen Recombinant protein of human VIM
Isotype Mouse IgG1
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):1:2,500-1:5,000
Immunocytochemistry (IC): 1:100-1:1,000
Flow Cytometry (FCM) : 1:2,000
Immunohistochemistry (IHC): 1:50-1:100
Note This product is for research use only.
Picture
  • Flow cytometric analysis of vimentin expression in HepG2 cells using anti-vimentin antibody (Cat#3471, 1:2,000). Green, isotype control; red, vimentin.
  • Immunocytochemical staining of HepG2 cells with anti-Vimentin antibody (Cat#3471, 1:1,000) . Nuclei were stained blue with DAPI; Vimentin was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and Smart Gain:Medium. Scale bar, 20 μm.
  • Immunohistochemistry was performed on paraffin-embedded human endometrial carcinoma using anti-vimentin antibody (Cat#3471, 1:100). 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.
  • Western blotting analysis using anti-vimentin antibody (Cat#3471). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-vimentin antibody (Cat#3471, 1:5,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit(Cat#716).
Citation(0)
Flow cytometric analysis of vimentin expression in HepG2 cells using anti-vimentin antibody (Cat#3471, 1:2,000). Green, isotype control; red, vimentin.
Immunocytochemical staining of HepG2 cells with anti-Vimentin antibody (Cat#3471, 1:1,000) . Nuclei were stained blue with DAPI; Vimentin was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and Smart Gain:Medium. Scale bar, 20 μm.
Immunohistochemistry was performed on paraffin-embedded human endometrial carcinoma using anti-vimentin antibody (Cat#3471, 1:100). 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.
Western blotting analysis using anti-vimentin antibody (Cat#3471). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-vimentin antibody (Cat#3471, 1:5,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit(Cat#716).
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