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KD-Validated Heat Shock Transcription Factor 1 Recombinant Rabbit mAb

#61469

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using Heat shock transcription factor 1 antibody (Cat#61469). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Heat shock transcription factor 1 antibody (Cat#61469, 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 Heat shock transcription factor 1 antibody (Cat#61469). Heat shock transcription factor 1 expression in wild type (WT) and heat shock transcription factor 1 shRNA knockdown (KD) 293T cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with Heat shock transcription factor 1 antibody (Cat#61469, 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 ovarian carcinoma using heat shock transcription factor 1 antibody (Cat#61469, 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 Heat shock transcription factor 1 antibody (Cat#61469, 1:1,000). Nuclei were stained blue with DAPI; Heat shock transcription factor 1 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 293T cells using Heat shock transcription factor 1 antibody (Cat#61469, 1:1,000), Top panel: wild-type (WT); Bottom panal: Heat shock transcription factor 1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; Heat shock transcription factor 1 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 Heat shock transcription factor 1 expression in HepG2 cells using Heat shock transcription factor 1 antibody (Cat#61469, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Heat shock transcription factor 1.
Validation of Heat shock transcription factor 1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) 293T cells were stained with Heat shock transcription factor 1 antibody (Cat#61469, 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
Quantity:
1
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  • Gene Symbol:
    HSF1
  • Catalog:
    61469
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H
Information
Product Name KD-Validated Heat Shock Transcription Factor 1 Recombinant Rabbit mAb
Aliases HSF1; Heat Shock Transcription Factor 1; HSTF1; Heat Shock Factor Protein 1; HSTF; HSF
Background

Gene Name: HSF1

NCBI Gene Entry: 3297

UniProt Entry: Q00613

Application Information

Molecular Weight: Predicted, 57 kDa; observed, 80 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB2715

Species Reactivity: Human

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

Immunogen A synthesized peptide derived from human HSF1
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 Heat shock transcription factor 1 antibody (Cat#61469). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Heat shock transcription factor 1 antibody (Cat#61469, 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 Heat shock transcription factor 1 antibody (Cat#61469). Heat shock transcription factor 1 expression in wild type (WT) and heat shock transcription factor 1 shRNA knockdown (KD) 293T cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with Heat shock transcription factor 1 antibody (Cat#61469, 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 ovarian carcinoma using heat shock transcription factor 1 antibody (Cat#61469, 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 Heat shock transcription factor 1 antibody (Cat#61469, 1:1,000). Nuclei were stained blue with DAPI; Heat shock transcription factor 1 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 293T cells using Heat shock transcription factor 1 antibody (Cat#61469, 1:1,000), Top panel: wild-type (WT); Bottom panal: Heat shock transcription factor 1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; Heat shock transcription factor 1 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 Heat shock transcription factor 1 expression in HepG2 cells using Heat shock transcription factor 1 antibody (Cat#61469, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Heat shock transcription factor 1.
  • Validation of Heat shock transcription factor 1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) 293T cells were stained with Heat shock transcription factor 1 antibody (Cat#61469, 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 Heat shock transcription factor 1 antibody (Cat#61469). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Heat shock transcription factor 1 antibody (Cat#61469, 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 Heat shock transcription factor 1 antibody (Cat#61469). Heat shock transcription factor 1 expression in wild type (WT) and heat shock transcription factor 1 shRNA knockdown (KD) 293T cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with Heat shock transcription factor 1 antibody (Cat#61469, 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 ovarian carcinoma using heat shock transcription factor 1 antibody (Cat#61469, 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 Heat shock transcription factor 1 antibody (Cat#61469, 1:1,000). Nuclei were stained blue with DAPI; Heat shock transcription factor 1 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 293T cells using Heat shock transcription factor 1 antibody (Cat#61469, 1:1,000), Top panel: wild-type (WT); Bottom panal: Heat shock transcription factor 1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; Heat shock transcription factor 1 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 Heat shock transcription factor 1 expression in HepG2 cells using Heat shock transcription factor 1 antibody (Cat#61469, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Heat shock transcription factor 1.
Validation of Heat shock transcription factor 1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) 293T cells were stained with Heat shock transcription factor 1 antibody (Cat#61469, 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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