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KD-Validated Syndecan Binding Protein Recombinant Rabbit mAb

#61201

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using Syndecan binding protein antibody (Cat#61201). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Syndecan binding protein antibody (Cat#61201, 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 syndecan binding protein antibody (Cat#61201). Syndecan binding protein expression in wild type (WT) and syndecan binding protein (SDCBP) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with syndecan binding protein antibody (Cat#61201, 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 hepatocarcinoma using syndecan binding protein antibody (Cat#61201, 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 Syndecan binding protein antibody(Cat#61201, 1:1,000). Nuclei were stained blue with DAPI; Syndecan binding protein was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: High. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Immunocytochemical staining of HeLa cells using syndecan binding protein antibody (Cat#61201, 1:1,000), Top panel: wild-type (WT); Bottom panal: Syndecan binding protein shRNA knockdown (KD). Nuclei were stained blue with DAPI; Syndecan binding protein was stained magenta with Alexa Fluor® 647. 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 Syndecan binding protein expression in HepG2 cells using Syndecan binding protein antibody (Cat#61201, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Syndecan binding protein.
Validation of Syndecan binding protein knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with Syndecan binding protein antibody (Cat#61201, 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:
    SDCBP
  • Catalog:
    61201
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H
Information
Product Name KD-Validated Syndecan Binding Protein Recombinant Rabbit mAb
Aliases SDCBP; Syndecan Binding Protein; MDA-9; SYCL; Syntenin-1; Pro-TGF-Alpha Cytoplasmic Domain-Interacting Protein 18; Syndecan-Binding Protein 1; Scaffold Protein Pbp1; TACIP18; SDCBP1; MDA9; Melanoma Differentiation Associated Protein-9; Melanoma Differentiation-Associated Protein 9; Syndecan Binding Protein (Syntenin); Syntenin; ST1
Background

Gene Name: SDCBP

NCBI Gene Entry: 6386

UniProt Entry: O00560

Application Information

Molecular Weight: Predicted, 32 kDa; observed, 32 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB2185

Species Reactivity: Human

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

Immunogen A synthesized peptide derived from human Syntenin
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 Syndecan binding protein antibody (Cat#61201). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Syndecan binding protein antibody (Cat#61201, 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 syndecan binding protein antibody (Cat#61201). Syndecan binding protein expression in wild type (WT) and syndecan binding protein (SDCBP) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with syndecan binding protein antibody (Cat#61201, 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 hepatocarcinoma using syndecan binding protein antibody (Cat#61201, 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 Syndecan binding protein antibody(Cat#61201, 1:1,000). Nuclei were stained blue with DAPI; Syndecan binding protein was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: High. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
  • Immunocytochemical staining of HeLa cells using syndecan binding protein antibody (Cat#61201, 1:1,000), Top panel: wild-type (WT); Bottom panal: Syndecan binding protein shRNA knockdown (KD). Nuclei were stained blue with DAPI; Syndecan binding protein was stained magenta with Alexa Fluor® 647. 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 Syndecan binding protein expression in HepG2 cells using Syndecan binding protein antibody (Cat#61201, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Syndecan binding protein.
  • Validation of Syndecan binding protein knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with Syndecan binding protein antibody (Cat#61201, 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 Syndecan binding protein antibody (Cat#61201). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Syndecan binding protein antibody (Cat#61201, 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 syndecan binding protein antibody (Cat#61201). Syndecan binding protein expression in wild type (WT) and syndecan binding protein (SDCBP) shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with syndecan binding protein antibody (Cat#61201, 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 hepatocarcinoma using syndecan binding protein antibody (Cat#61201, 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 Syndecan binding protein antibody(Cat#61201, 1:1,000). Nuclei were stained blue with DAPI; Syndecan binding protein was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: High. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Immunocytochemical staining of HeLa cells using syndecan binding protein antibody (Cat#61201, 1:1,000), Top panel: wild-type (WT); Bottom panal: Syndecan binding protein shRNA knockdown (KD). Nuclei were stained blue with DAPI; Syndecan binding protein was stained magenta with Alexa Fluor® 647. 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 Syndecan binding protein expression in HepG2 cells using Syndecan binding protein antibody (Cat#61201, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Syndecan binding protein.
Validation of Syndecan binding protein knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with Syndecan binding protein antibody (Cat#61201, 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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