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

KD-Validated MacroH2A.1 Histone Recombinant Rabbit mAb

#61249

Click to copy product information
Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using macroH2A.1 Histone antibody (Cat#61249). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with macroH2A.1 Histone antibody (Cat#61249, 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).
Western blotting analysis using macroH2A.1 histone antibody (Cat#61249). MacroH2A.1 histone expression in wild type (WT) and macroH2A.1 histone (H2AFY) shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with macroH2A.1 histone antibody (Cat#61249, 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 skin tissue using macroH2A.1 histone antibody (Cat#61249, 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 macroH2A.1 Histone antibody (Cat#61249, 1:1,000), Top panel: wild-type (WT); Bottom panal: MacroH2A.1 Histone shRNA knockdown (KD). Nuclei were stained blue with DAPI; MacroH2A.1 Histone 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.
Immunocytochemical staining of HAP-1 cells with macroH2A.1 Histone antibody (Cat#61249, 1:1,000). Nuclei were stained blue with DAPI; MacroH2A.1 Histone 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 macroH2A.1 Histone expression in HAP-1 cells using macroH2A.1 Histone antibody (Cat#61249, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, MacroH2A.1 Histone.
Validation of macroH2A.1 Histone knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with macroH2A.1 Histone antibody (Cat#61249, 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.
Please select the specifications of the product.
Specification:
Unit price:
$89.00
Quantity:
1
(Excluding sales tax)
  • Gene Symbol:
    MACROH2A1
  • Catalog:
    61249
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, M, R
Information
Product Name KD-Validated MacroH2A.1 Histone Recombinant Rabbit mAb
Aliases MACROH2A1; MacroH2A.1 Histone; H2AFY; Medulloblastoma Antigen MU-MB-50.205; H2A Histone Family Member Y; Core Histone Macro-H2A.1; Histone MacroH2A1; Histone H2A.Y; MacroH2A1.2; H2A/Y; MH2A1; H2A Histone Family, Member Y; Histone MacroH2A1.1; Histone MacroH2A1.2; MACROH2A1.1; MACROH2A1.2; H2AF12M; H2A.Y
Background

Gene Name: MACROH2A1

NCBI Gene Entry: 9555

UniProt Entry: O75367

Application Information

Molecular Weight: Predicted, 40 kDa; observed, 40 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 25GB485

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 macroH2A.1
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 macroH2A.1 Histone antibody (Cat#61249). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with macroH2A.1 Histone antibody (Cat#61249, 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).
  • Western blotting analysis using macroH2A.1 histone antibody (Cat#61249). MacroH2A.1 histone expression in wild type (WT) and macroH2A.1 histone (H2AFY) shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with macroH2A.1 histone antibody (Cat#61249, 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 skin tissue using macroH2A.1 histone antibody (Cat#61249, 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 macroH2A.1 Histone antibody (Cat#61249, 1:1,000), Top panel: wild-type (WT); Bottom panal: MacroH2A.1 Histone shRNA knockdown (KD). Nuclei were stained blue with DAPI; MacroH2A.1 Histone 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.
  • Immunocytochemical staining of HAP-1 cells with macroH2A.1 Histone antibody (Cat#61249, 1:1,000). Nuclei were stained blue with DAPI; MacroH2A.1 Histone 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 macroH2A.1 Histone expression in HAP-1 cells using macroH2A.1 Histone antibody (Cat#61249, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, MacroH2A.1 Histone.
  • Validation of macroH2A.1 Histone knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with macroH2A.1 Histone antibody (Cat#61249, 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 macroH2A.1 Histone antibody (Cat#61249). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with macroH2A.1 Histone antibody (Cat#61249, 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).
Western blotting analysis using macroH2A.1 histone antibody (Cat#61249). MacroH2A.1 histone expression in wild type (WT) and macroH2A.1 histone (H2AFY) shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with macroH2A.1 histone antibody (Cat#61249, 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 skin tissue using macroH2A.1 histone antibody (Cat#61249, 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 macroH2A.1 Histone antibody (Cat#61249, 1:1,000), Top panel: wild-type (WT); Bottom panal: MacroH2A.1 Histone shRNA knockdown (KD). Nuclei were stained blue with DAPI; MacroH2A.1 Histone 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.
Immunocytochemical staining of HAP-1 cells with macroH2A.1 Histone antibody (Cat#61249, 1:1,000). Nuclei were stained blue with DAPI; MacroH2A.1 Histone 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 macroH2A.1 Histone expression in HAP-1 cells using macroH2A.1 Histone antibody (Cat#61249, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, MacroH2A.1 Histone.
Validation of macroH2A.1 Histone knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with macroH2A.1 Histone antibody (Cat#61249, 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.
  • 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.