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KD-Validated IGF2R Recombinant Rabbit mAb

#61979

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using IGF2R antibody (Cat#61979). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with IGF2R antibody (Cat#61979, 1:20,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using IGF2R antibody (Cat#61979). IGF2R expression in wild-type (WT) and IGF2R shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with IGF2R antibody (Cat#61979, 1:20,000) 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 prostatic adenocarcinoma using IGF2R antibody (Cat#61979, 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.
Immunohistochemistry was performed on paraffin-embedded mouse colon tissue using IGF2R antibody (Cat#61979, 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 HeLa cells using IGF2R antibody (Cat#61979, 1:1,000), Top panel: wild-type (WT); Bottom panal: IGF2R shRNA knockdown (KD). Nuclei were stained blue with DAPI; IGF2R 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.
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Specification:
Unit price:
$89.00
Quantity:
1
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  • Gene Symbol:
    IGF2R
  • Catalog:
    61979
  • Application:
    WB, ICC, IHC-P
  • Species Reactivity:
    H, M
Information
Product Name KD-Validated IGF2R Recombinant Rabbit mAb
Aliases IGF2R; Insulin Like Growth Factor 2 Receptor; MPRI; CI-M6PR; CI-MPR; MPR300; CD222; CIMPR; M6P-R; MPR1; Cation-Independent Mannose-6-Phosphate Receptor; Insulin-Like Growth Factor II Receptor; Insulin-Like Growth Factor 2 Receptor; 300 KDa Mannose 6-Phosphate Receptor; CI Man-6-P Receptor; M6P/IGF2 Receptor; IGF-II Receptor; M6P/IGF2R; MPR 300; Cation-Independent Mannose-6 Phosphate Receptor; CD222 Antigen; M6PR
Background

Gene Name: IGF2R

NCBI Gene Entry: 3482

UniProt Entry: P11717

Application Information

Molecular Weight: Predicted, 274 kDa; observed, 300 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 25GB6790

Species Reactivity: Human,mouse

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

Immunogen A synthesized peptide derived from human M6PR/IGF2R
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): 1:4,000-1:20,000
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 IGF2R antibody (Cat#61979). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with IGF2R antibody (Cat#61979, 1:20,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
  • Western blotting analysis using IGF2R antibody (Cat#61979). IGF2R expression in wild-type (WT) and IGF2R shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with IGF2R antibody (Cat#61979, 1:20,000) 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 prostatic adenocarcinoma using IGF2R antibody (Cat#61979, 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.
  • Immunohistochemistry was performed on paraffin-embedded mouse colon tissue using IGF2R antibody (Cat#61979, 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 HeLa cells using IGF2R antibody (Cat#61979, 1:1,000), Top panel: wild-type (WT); Bottom panal: IGF2R shRNA knockdown (KD). Nuclei were stained blue with DAPI; IGF2R 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.
Western blotting analysis using IGF2R antibody (Cat#61979). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with IGF2R antibody (Cat#61979, 1:20,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using IGF2R antibody (Cat#61979). IGF2R expression in wild-type (WT) and IGF2R shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with IGF2R antibody (Cat#61979, 1:20,000) 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 prostatic adenocarcinoma using IGF2R antibody (Cat#61979, 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.
Immunohistochemistry was performed on paraffin-embedded mouse colon tissue using IGF2R antibody (Cat#61979, 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 HeLa cells using IGF2R antibody (Cat#61979, 1:1,000), Top panel: wild-type (WT); Bottom panal: IGF2R shRNA knockdown (KD). Nuclei were stained blue with DAPI; IGF2R 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.
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