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EZH1 Recombinant Rabbit Monoclonal Antibody [PS01-09] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA750521

EZH1 Recombinant Rabbit Monoclonal Antibody [PS01-09] - BSA and Azide free

Application

  • WB

  • IHC-P

  • IF-Cell

Reactivity

  • Human

  • Mouse

  • Rat

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

EZH1 Recombinant Rabbit Monoclonal Antibody [PS01-09] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Synthetic peptide within human EZH1 aa 471-510/747.

Species Reactivity

Human, Mouse, Rat

Validated Applications

WB, IHC-P, IF-Cell

Target Molecular Weight

Predicted band size: 85 kDa

Positive Control

HCT 116 cell lysate, K-562 cell lysate, PANC-1 cell lysate, NIH/3T3 cell lysate, PC-12 cell lysate, rat large intestine tissue, mouse large intestine tissue, HCT 116.

Conjugation

unconjugated

Clone Number

PS01-09

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

Target

Function

Histone-lysine N-methyltransferase EZH1 is an enzyme that in humans is encoded by the EZH1 gene. In mice, EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair. EZH1 also complements EZH2 in maintaining stem cell identity and executing pluripotency.

Background References

1. Utsunomiya S et al. Ezh1 regulates expression of Cpg15/Neuritin in mouse cortical neurons. Drug Discov Ther. 2021 May

2. Kusakabe Y et al. EZH1/2 inhibition augments the anti-tumor effects of sorafenib in hepatocellular carcinoma. Sci Rep. 2021 Nov

Subcellular Location

Nucleus.

UNIPROT

SwissProt: Q92800 Human

SwissProt: P70351 Mouse

Entrez Gene: 303547 Rat

Synonyms

Enhancer of zeste homolog 1 (Drosophila) antibody

Enhancer of zeste homolog 1 antibody

ENX-2 antibody

ENX2 antibody

Ezh1 antibody

EZH1_HUMAN antibody

Histone-lysine N-methyltransferase EZH1 antibody

Images

  • This data was developed using <a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of EZH1 on different lysates with Rabbit anti-EZH1 antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/1,000 dilution.<br /><br />Lane 1: HCT 116 cell lysate (20 µg/Lane)<br />Lane 2: K-562 cell lysate (20 µg/Lane)<br />Lane 3: PANC-1 cell lysate (20 µg/Lane)<br />Lane 4: NIH/3T3 cell lysate (17 µg/Lane)<br />Lane 5: PC-12 cell lysate (20 µg/Lane)<br /><br />Predicted band size: 85 kDa<br />Observed band size: 85/110 kDa<br /><br />Exposure time: 3 minutes;<br />4-20% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1:300,000 dilution was used for 1 hour at room temperature.

    This data was developed using HA721187, the same antibody clone in a different buffer formulation.
    Western blot analysis of EZH1 on different lysates with Rabbit anti-EZH1 antibody (HA721187) at 1/1,000 dilution.

    Lane 1: HCT 116 cell lysate (20 µg/Lane)
    Lane 2: K-562 cell lysate (20 µg/Lane)
    Lane 3: PANC-1 cell lysate (20 µg/Lane)
    Lane 4: NIH/3T3 cell lysate (17 µg/Lane)
    Lane 5: PC-12 cell lysate (20 µg/Lane)

    Predicted band size: 85 kDa
    Observed band size: 85/110 kDa

    Exposure time: 3 minutes;
    4-20% SDS-PAGE gel.

    Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721187) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature.

  • This data was developed using <a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded rat large intestine tissue with Rabbit anti-EZH1 antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/2,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    This data was developed using HA721187, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded rat large intestine tissue with Rabbit anti-EZH1 antibody (HA721187) at 1/2,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721187) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • This data was developed using <a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>, the same antibody clone in a different buffer formulation.<br />Immunohistochemical analysis of paraffin-embedded mouse large intestine tissue with Rabbit anti-EZH1 antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/2,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    This data was developed using HA721187, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded mouse large intestine tissue with Rabbit anti-EZH1 antibody (HA721187) at 1/2,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721187) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • This data was developed using <a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>, the same antibody clone in a different buffer formulation.<br />Immunocytochemistry analysis of HCT 116 cells labeling EZH1 with Rabbit anti-EZH1 antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/200 dilution.<br /><br />Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-EZH1 antibody (<a href="/products/HA721187" style="font-weight: bold;text-decoration: underline;">HA721187</a>) at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor&trade; 488, <a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

    This data was developed using HA721187, the same antibody clone in a different buffer formulation.
    Immunocytochemistry analysis of HCT 116 cells labeling EZH1 with Rabbit anti-EZH1 antibody (HA721187) at 1/200 dilution.

    Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-EZH1 antibody (HA721187) at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

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