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KD-Validated TACC3 Recombinant Rabbit mAb

#62642

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using TACC3 antibody (Cat#62642). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with TACC3 antibody (Cat#62642, 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 TACC3 antibody (Cat#62642). TACC3 expression in wild type (WT) and TACC3 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with TACC3 antibody (Cat#62642, 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 tonsillitis using TACC3 antibody (Cat#62642, 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 TACC3 antibody (Cat#62642, 1:1,000). Nuclei were stained blue with DAPI; TACC3 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.
Immunocytochemical staining of Hela cells using TACC3 antibody (Cat#62642, 1:1,000), Top panel: wild-type (WT); Bottom panal:TACC3 shRNA knockdown (KD). Nuclei were stained blue with DAPI;TACC3 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 TACC3 expression in HAP-1 cells using TACC3 antibody (Cat#62642, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, TACC3.
Validation of TACC3 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with TACC3 antibody (Cat#62642, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
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Unit price:
$89.00
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  • Gene Symbol:
    TACC3
  • Catalog:
    62642
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, R
Information
Product Name KD-Validated TACC3 Recombinant Rabbit mAb
Aliases TACC3; Transforming Acidic Coiled-Coil Containing Protein 3; ERIC-1; ERIC1; Maskin; Tacc4; Transforming Acidic Coiled-Coil-Containing Protein 3; Transforming, Acidic Coiled-Coil Containing Protein 3
Background

Gene Name: TACC3

NCBI Gene Entry: 10460

UniProt Entry: Q9Y6A5

Application Information

Molecular Weight: Predicted, 90 kDa; observed, 140 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 24GB1940

Species Reactivity: Human,rat

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

Immunogen A synthesized peptide derived from human TACC3
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 TACC3 antibody (Cat#62642). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with TACC3 antibody (Cat#62642, 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 TACC3 antibody (Cat#62642). TACC3 expression in wild type (WT) and TACC3 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with TACC3 antibody (Cat#62642, 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 tonsillitis using TACC3 antibody (Cat#62642, 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 TACC3 antibody (Cat#62642, 1:1,000). Nuclei were stained blue with DAPI; TACC3 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.
  • Immunocytochemical staining of Hela cells using TACC3 antibody (Cat#62642, 1:1,000), Top panel: wild-type (WT); Bottom panal:TACC3 shRNA knockdown (KD). Nuclei were stained blue with DAPI;TACC3 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 TACC3 expression in HAP-1 cells using TACC3 antibody (Cat#62642, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, TACC3.
  • Validation of TACC3 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with TACC3 antibody (Cat#62642, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
Western blotting analysis using TACC3 antibody (Cat#62642). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with TACC3 antibody (Cat#62642, 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 TACC3 antibody (Cat#62642). TACC3 expression in wild type (WT) and TACC3 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with TACC3 antibody (Cat#62642, 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 tonsillitis using TACC3 antibody (Cat#62642, 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 TACC3 antibody (Cat#62642, 1:1,000). Nuclei were stained blue with DAPI; TACC3 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.
Immunocytochemical staining of Hela cells using TACC3 antibody (Cat#62642, 1:1,000), Top panel: wild-type (WT); Bottom panal:TACC3 shRNA knockdown (KD). Nuclei were stained blue with DAPI;TACC3 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 TACC3 expression in HAP-1 cells using TACC3 antibody (Cat#62642, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, TACC3.
Validation of TACC3 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with TACC3 antibody (Cat#62642, 1:2,000) and analyzed using BD flow cytometer. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS.
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