Copy Link Print Information

Acetyl Lysine Antibody (YA6425)

(Synonyms: Acetylated Lysine; Acetyllysine; Ac-lysine; Ac lysine; Ac-K; Ac K; Ac-Lys; Ac Lys; acetyl-Lysine; acetyl Lys; Ac-Lysine; )
Customer Review

Based on 1 Customer Validation

Acetyl Lysine Antibody (YA6425) is a Mouse-derived and non-conjugated IgG monoclonal antibody, targeting to Acetyl Lysine.

For research use only. We do not sell to patients.
  • Host:

    Mouse

  • Isotype:

    IgG

  • Application:

    IHC-P, IHC-F, ICC/IF, IF-Tissue, FC

  • Reactivity :

    Species independent

  • Formulation:

    Supplied in 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

  • Conjugation:
    Non-conjugated
IHC-P
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Acetyl Lysine Antibody (YA6425) Product Image
Size
Price
Stock
Quantity
Amount: USD 0.00
Please select quantity
or
or

* Please select Quantity before adding items.

To place orders, for customer services and technical support, please contact: MedChemExpress USA

Tel: 609-228-6898 E-mail: [email protected] [email protected]

Service
Data Download
Related Products:
Top Publications Citing

Use of MCE Products

Applications

Application
IHC-P Info
IHC-P: Immunohistochemistry-Paraffin
IHC-F Info
IHC-F: Immunohistochemistry-Frozen
ICC/IF Info
ICC/IF: Immunocytochemistry/
Immunofluorescence
IF Info
 
FC Info
FC: Flow Cytometry
Dilution Ratio 1:100-500 1:100-500 1:50-200 1:100-500 1μg/Test

Product Details

Description

Acetyl Lysine Antibody (YA6425) is a Mouse-derived and non-conjugated IgG monoclonal antibody, targeting to Acetyl Lysine.

  • Host Mouse
  • Clonality Monoclonal
  • Species Reactivity
    Species independent Predicted Reactivity: Human
    Info
    Note: The predicted reactivity is for reference only and should not be considered a guarantee of product performance.
Immunogen

BSA conjugated Acetylated Lysine

Purification

affinity purified.

Conjugation

Non-conjugated

Modification

Unmodified

Isotype

IgG

Product Properties

  • Appearance

    Solution

  • Formulation

    Supplied in 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

  • Concentration

    Batch-dependent, Please check the COA for the concentration of each lot. Check Lot Concentration

  • Storage & Stability

    Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.

  • Shipping

    Shipping with blue ice.

Verification Images

  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    Immunohistochemical analysis of paraffin-embedded rat liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    Immunohistochemical analysis of paraffin-embedded mouse liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

Background

  • Function

    Acetyl Lysine is an Acetyl-L-lysine (HY-W048838)：Acetyl-L-lysine is an acetylated form of the amino acid L-lysine. Acetyl-L-lysine can participate in protein acylation processes, affecting protein functions such as stability and enzyme activity.

  • Synonyms

    Acetylated Lysine; Acetyllysine; Ac-lysine; Ac lysine; Ac-K; Ac K; Ac-Lys; Ac Lys; acetyl-Lysine; acetyl Lys; Ac-Lysine;

Acetyl Lysine Antibody (YA6425) Related Classifications

MOQ
Minimum order quantity
100 mg

Get Quote In-stock

Other size
Get Quote
Please select quantity
Amount: USD 0.00

Measured by its ability to inhibit anti-CD3-induced proliferation of stimulated CTLL-2 mouse cytotoxic T cells. The ED50 this effect is 0.8023 μg/ml, corresponding to a specific activity is 1246.42 units/mg.

Assay Types
  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded rat liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded mouse liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • Acetyl Lysine Antibody (YA6425) Product Image
    1/16
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Acetyl Lysine Antibody (YA6425) Product Image
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded rat liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded mouse liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Experimental Validation Results for Acetyl Lysine Antibody (YA6425)
  • Acetyl Lysine Antibody (YA6425) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • Acetyl Lysine Antibody (YA6425) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • Acetyl Lysine Antibody (YA6425) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded rat liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • Acetyl Lysine Antibody (YA6425) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded mouse liver tissue using Acetyl Lysine Antibody (HY-P86733, 1/100). The section was pretreated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 15 minutes. The tissues were blocked with quick block buffer for 0.5 hours at room temperature, washed with PBS and PBST, and then incubated with the primary antibody overnight at 4℃. 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.

  • Acetyl Lysine Antibody (YA6425) Product Image IHC-P
  • Acetyl Lysine Antibody (YA6425) Product Image IHC-P
  • Acetyl Lysine Antibody (YA6425) Product Image IHC-P
  • Acetyl Lysine Antibody (YA6425) Product Image IHC-P