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KO-Validated Progesterone Receptor Recombinant Rabbit mAb

#71202

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Recombinant Antibody
Knockout Validated
Western blotting analysis using progesterone receptor antibody (Cat#71202). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with progesterone receptor antibody (Cat#71202, 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 progesterone receptor antibody (Cat#71202). Progesterone receptor expression in wild type (WT) and progesterone receptor (PGR) knockout (KO) HSHC cells with 50 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with progesterone receptor antibody (Cat#71202, 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 breast carcinoma using progesterone receptor antibody (Cat#71202, 1:200). Antigen retrieval was done in EDTA buffer (pH 9.0). 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 H9C2 cells with Progesterone receptor antibody (Cat#71202, 1:1,000). Nuclei were stained blue with DAPI; Progesterone receptor 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.
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  • Gene Symbol:
    PGR
  • Catalog:
    71202
  • Application:
    WB, ICC, IHC-P
  • Species Reactivity:
    H
Information
Product Name KO-Validated Progesterone Receptor Recombinant Rabbit mAb
Aliases PGR; Progesterone Receptor; NR3C3; PR; Nuclear Receptor Subfamily 3 Group C Member 3
Background

Gene Name: PGR

NCBI Gene Entry: 5241

UniProt Entry: P06401

Application Information

Molecular Weight: Predicted, 99 kDa; observed, 120 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 25GB2650

Species Reactivity: Human

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

Immunogen A synthesized peptide derived from human Progesterone Receptor
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
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 progesterone receptor antibody (Cat#71202). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with progesterone receptor antibody (Cat#71202, 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 progesterone receptor antibody (Cat#71202). Progesterone receptor expression in wild type (WT) and progesterone receptor (PGR) knockout (KO) HSHC cells with 50 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with progesterone receptor antibody (Cat#71202, 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 breast carcinoma using progesterone receptor antibody (Cat#71202, 1:200). Antigen retrieval was done in EDTA buffer (pH 9.0). 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 H9C2 cells with Progesterone receptor antibody (Cat#71202, 1:1,000). Nuclei were stained blue with DAPI; Progesterone receptor 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.
Western blotting analysis using progesterone receptor antibody (Cat#71202). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with progesterone receptor antibody (Cat#71202, 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 progesterone receptor antibody (Cat#71202). Progesterone receptor expression in wild type (WT) and progesterone receptor (PGR) knockout (KO) HSHC cells with 50 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with progesterone receptor antibody (Cat#71202, 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 breast carcinoma using progesterone receptor antibody (Cat#71202, 1:200). Antigen retrieval was done in EDTA buffer (pH 9.0). 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 H9C2 cells with Progesterone receptor antibody (Cat#71202, 1:1,000). Nuclei were stained blue with DAPI; Progesterone receptor 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.
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