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KD-Validated KMT6/EZH2 Recombinant Rabbit mAb

#69932

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Recombinant Antibody
shRNA Knockdown Validated
Western blotting analysis using KMT6 / EZH2 antibody (Cat#69932). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with KMT6 / EZH2 antibody (Cat#69932, 1:10,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:50,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using KMT6 / EZH2 antibody (Cat#69932).KMT6 / EZH2 expression in wild type (WT) and KMT6 / EZH2 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with KMT6 / EZH2 antibody (Cat#69932, 1:10,000) 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 breast carcinoma using KMT6 / EZH2 antibody (Cat#69932, 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 HepG2 cells with KMT6 / EZH2 antibody (Cat#69932, 1:1,000). Nuclei were stained blue with DAPI; KMT6 / EZH2 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 KMT6 / EZH2 expression in HepG2 cells using KMT6 / EZH2 antibody (Cat#69932, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, KMT6 / EZH2.
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  • Gene Symbol:
    EZH2
  • Catalog:
    69932
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, M, R
Information
Product Name KD-Validated KMT6/EZH2 Recombinant Rabbit mAb
Aliases Enhancer Of Zeste 2 Polycomb Repressive Complex 2 Subunit; ENX-1; KMT6; KMT6A; Histone-Lysine N-Methyltransferase EZH2; Lysine N-Methyltransferase 6; Enhancer Of Zeste Homolog 2;EZH1; Enhancer Of Zeste (Drosophila) Homolog 2; Enhancer Of Zeste Homolog 2 (Drosophila); EC 2.1.1.356; EC 2.1.1.43; EC 2.1.1; EZH2b; ENX1; WVS2; WVS
Background

Gene Name: EZH2

NCBI Gene Entry: 2146

UniProt Entry: Q15910

Application Information

Molecular Weight: Predicted, 85 kDa; observed, 98 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 23GB835

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 KMT6 / EZH2
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): 1:2,000-1:10,000
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 KMT6 / EZH2 antibody (Cat#69932). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with KMT6 / EZH2 antibody (Cat#69932, 1:10,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:50,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using KMT6 / EZH2 antibody (Cat#69932).KMT6 / EZH2 expression in wild type (WT) and KMT6 / EZH2 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with KMT6 / EZH2 antibody (Cat#69932, 1:10,000) 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 breast carcinoma using KMT6 / EZH2 antibody (Cat#69932, 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 HepG2 cells with KMT6 / EZH2 antibody (Cat#69932, 1:1,000). Nuclei were stained blue with DAPI; KMT6 / EZH2 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 KMT6 / EZH2 expression in HepG2 cells using KMT6 / EZH2 antibody (Cat#69932, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, KMT6 / EZH2.
Western blotting analysis using KMT6 / EZH2 antibody (Cat#69932). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with KMT6 / EZH2 antibody (Cat#69932, 1:10,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:50,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using KMT6 / EZH2 antibody (Cat#69932).KMT6 / EZH2 expression in wild type (WT) and KMT6 / EZH2 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with KMT6 / EZH2 antibody (Cat#69932, 1:10,000) 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 breast carcinoma using KMT6 / EZH2 antibody (Cat#69932, 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 HepG2 cells with KMT6 / EZH2 antibody (Cat#69932, 1:1,000). Nuclei were stained blue with DAPI; KMT6 / EZH2 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 KMT6 / EZH2 expression in HepG2 cells using KMT6 / EZH2 antibody (Cat#69932, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, KMT6 / EZH2.
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