• Primary Antibody
  • Secondary Antibodies
  • Lentiviral Particles
  • Stable Cell Lines
  • Lysates
  • Reagents
  • Other Products

IGF2BP2 Recombinant Rabbit mAb

#2091

Click to copy product information
Recombinant Antibody
Western blotting analysis using IGF2BP2 antibody (Cat#2091). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with IGF2BP2 antibody (Cat#2091, 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 sigmoid colon carcinoma sections using IGF2BP2 antibody (Cat#2091, 1:1,000). Antigen retrieval was carried out in sodium citrate buffer (pH 6.0). Nuclei were counterstained with DAPI (blue), and IGF2BP2 was visualized with Alexa Fluor® 647 (magenta). Protein abundance, based on laser intensity and smart gain settings, was classified as medium. Images were acquired using a Leica Stellaris 5 confocal microscope. Scale bar: 20 µm.
Immunohistochemistry was performed on paraffin-embedded mouse liver using IGF2BP2 antibody (Cat#2091, 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 brain sections using IGF2BP2 antibody (Cat#2091, 1:1,000). Antigen retrieval was carried out in sodium citrate buffer (pH 6.0). Nuclei were counterstained with DAPI (blue), and IGF2BP2 was visualized with Alexa Fluor® 647 (magenta). Protein abundance, based on laser intensity and smart gain settings, was classified as medium. Images were acquired using a Leica Stellaris 5 confocal microscope. Scale bar: 20 µm.
Immunocytochemical staining of HAP-1 cells with IGF2BP2 antibody (Cat#2091, 1:1,000). Nuclei were stained blue with DAPI;IGF2BP2 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.
Flow cytometric analysis of IGF2BP2 expression in HAP-1 cells using IGF2BP2 antibody (Cat#2091, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, IGF2BP2.
Please select the specifications of the product.
Specification:
Unit price:
$69.00
Quantity:
1
(Excluding sales tax)
  • Gene Symbol:
    IGF2BP2
  • Catalog:
    2091
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, M, R
Information
Product Name IGF2BP2 Recombinant Rabbit mAb
Aliases IGF2BP2; Insulin Like Growth Factor 2 MRNA Binding Protein 2; IMP-2; P62; Insulin-Like Growth Factor 2 MRNA-Binding Protein; IGF-II MRNA-Binding Protein 2; IGF2 MRNA-Binding Protein; VICKZ Family Member 2; VICKZ2; IMP2; Insulin-Like Growth Factor 2 MRNA Binding Protein 2; Hepatocellular Carcinoma Autoantigen P62; IGF II MRNA Binding Protein 2
Background

Gene Name: IGF2BP2

NCBI Gene Entry: 10644

UniProt Entry: Q9Y6M1

Application Information

Molecular Weight: Predicted, 66 kDa; observed, 66 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB5955

Species Reactivity: Human,mouse,rat

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

Immunogen A synthesized peptide derived from human IGF2BP2
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 IGF2BP2 antibody (Cat#2091). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with IGF2BP2 antibody (Cat#2091, 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 sigmoid colon carcinoma sections using IGF2BP2 antibody (Cat#2091, 1:1,000). Antigen retrieval was carried out in sodium citrate buffer (pH 6.0). Nuclei were counterstained with DAPI (blue), and IGF2BP2 was visualized with Alexa Fluor® 647 (magenta). Protein abundance, based on laser intensity and smart gain settings, was classified as medium. Images were acquired using a Leica Stellaris 5 confocal microscope. Scale bar: 20 µm.
  • Immunohistochemistry was performed on paraffin-embedded mouse liver using IGF2BP2 antibody (Cat#2091, 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 brain sections using IGF2BP2 antibody (Cat#2091, 1:1,000). Antigen retrieval was carried out in sodium citrate buffer (pH 6.0). Nuclei were counterstained with DAPI (blue), and IGF2BP2 was visualized with Alexa Fluor® 647 (magenta). Protein abundance, based on laser intensity and smart gain settings, was classified as medium. Images were acquired using a Leica Stellaris 5 confocal microscope. Scale bar: 20 µm.
  • Immunocytochemical staining of HAP-1 cells with IGF2BP2 antibody (Cat#2091, 1:1,000). Nuclei were stained blue with DAPI;IGF2BP2 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.
  • Flow cytometric analysis of IGF2BP2 expression in HAP-1 cells using IGF2BP2 antibody (Cat#2091, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, IGF2BP2.
Western blotting analysis using IGF2BP2 antibody (Cat#2091). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with IGF2BP2 antibody (Cat#2091, 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 sigmoid colon carcinoma sections using IGF2BP2 antibody (Cat#2091, 1:1,000). Antigen retrieval was carried out in sodium citrate buffer (pH 6.0). Nuclei were counterstained with DAPI (blue), and IGF2BP2 was visualized with Alexa Fluor® 647 (magenta). Protein abundance, based on laser intensity and smart gain settings, was classified as medium. Images were acquired using a Leica Stellaris 5 confocal microscope. Scale bar: 20 µm.
Immunohistochemistry was performed on paraffin-embedded mouse liver using IGF2BP2 antibody (Cat#2091, 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 brain sections using IGF2BP2 antibody (Cat#2091, 1:1,000). Antigen retrieval was carried out in sodium citrate buffer (pH 6.0). Nuclei were counterstained with DAPI (blue), and IGF2BP2 was visualized with Alexa Fluor® 647 (magenta). Protein abundance, based on laser intensity and smart gain settings, was classified as medium. Images were acquired using a Leica Stellaris 5 confocal microscope. Scale bar: 20 µm.
Immunocytochemical staining of HAP-1 cells with IGF2BP2 antibody (Cat#2091, 1:1,000). Nuclei were stained blue with DAPI;IGF2BP2 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.
Flow cytometric analysis of IGF2BP2 expression in HAP-1 cells using IGF2BP2 antibody (Cat#2091, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, IGF2BP2.
  • Phone Number

    +1 (301) 545-2395

  • Email Address

    support@genuinbiotech.com

    sales@genuinbiotech.com

  • Office Hours

    8:30 AM - 5:30 PM EST Mon-Fri

微信公众号

Copyright © 2025 Hefei GenuIN Biotech Co., Ltd.

All Rights Reserved.