Copy Link Print Information

Aspartate Aminotransferase Antibody (YA2175)

(Synonyms: Aspartate aminotransferase; cytoplasmic; Glutamate oxaloacetate transaminase 1; Transaminase A)
Customer Review

Based on 1 Customer Validation

Aspartate Aminotransferase Antibody (YA2175) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Aspartate Aminotransferase.

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

    Rabbit

  • Isotype:

    IgG

  • Application:

    WB, IHC-F, IHC-P, ICC/IF

  • Reactivity :

    Human, Mouse, Rat

  • Formulation:

    Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA

  • Conjugation:
    Non-conjugated
ALL WB IHC-P
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Aspartate Aminotransferase Antibody (YA2175) 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
WB Info
WB: Western Blot
IHC-P Info
IHC-P: Immunohistochemistry-Paraffin
IHC-F Info
IHC-F: Immunohistochemistry-Frozen
ICC/IF Info
ICC/IF: Immunocytochemistry/
Immunofluorescence
Dilution Ratio 1:500-1:1000 1:50-1:100 1:50-1:100 1:50-1:200

Product Details

Description

Aspartate Aminotransferase Antibody (YA2175) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Aspartate Aminotransferase.

  • Host Rabbit
  • Clonality Recombinant,Monoclonal
  • Species Reactivity
    Human, Mouse, Rat
  • Observed Molecular Weight
    Observed band size: 46 kDa Info
    Note: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
  • Calculated Molecular Weight Predicted band size: 46 kDa
Species Reactivity Database
Immunogen

A synthetic peptide of human Aspartate Aminotransferase aa197-210.

Sensitivity

Endogenous

Purification

Affinity Purified

Conjugation

Non-conjugated

Modification

Unmodified

Isotype

IgG

RRID

AB_3104539

Product Properties

  • Appearance

    Liquid

  • Formulation

    Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA

  • 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 Aspartate Aminotransferase Antibody (YA2175)
    Western blot analysis of extracts from A549 (lane 2(20μg)), Hela (lane 3(20μg)), LNcap (lane 4(20μg)), Mouse brain (lane 4(20μg)) and Rat brain (lane 5(20μg)) using Aspartate Aminotransferase Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (beta Actin, HY-P83730, 1/5000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Rabbit/Mouse IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human Prostate cancer‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human Stromal tumor‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human placenta tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human serous ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human Uterine leiomyoma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human fibroma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    Immunohistochemical analysis of paraffin-embedded human aggressive fibromatosis tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

Background

  • Function

    Aspartate Aminotransferase is a Biosynthesis of L-glutamate from L-aspartate or L-cysteine. Important regulator of levels of glutamate, the major excitatory neurotransmitter of the vertebrate central nervous system. Acts as a scavenger of glutamate in brain neuroprotection. The aspartate aminotransferase activity is involved in hepatic glucose synthesis during development and in adipocyte glyceroneogenesis. Using L-cysteine as substrate, regulates levels of mercaptopyruvate, an important source of hydrogen sulfide. Mercaptopyruvate is converted into H(2)S via the action of 3-mercaptopyruvate sulfurtransferase (3MST). Hydrogen sulfide is an important synaptic modulator and neuroprotectant in the brain. In addition, catalyzes (2S)-2-aminobutanoate, a by-product in the cysteine biosynthesis pathway[1][2].

  • Subcellular Localization

    Cytoplasm

  • Isoforms & Post-Translational Modification

    P17174 has 2 isomers: P17174-1: 46248 Da (predicted); P17174-2: 44147 Da (predicted).

  • Subunit

    Homodimer

  • SwissProt ID

    P17174

  • Gene ID
    2805 [NCBI]
  • Synonyms

    Aspartate aminotransferase; cytoplasmic; Glutamate oxaloacetate transaminase 1; Transaminase A

  • Research Field

    Signal Transduction

Aspartate Aminotransferase Antibody (YA2175) 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
     Western blot analysis of extracts from A549 (lane 2(20μg)), Hela (lane 3(20μg)), LNcap (lane 4(20μg)), Mouse brain (lane 4(20μg)) and Rat brain (lane 5(20μg)) using Aspartate Aminotransferase Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (beta Actin, HY-P83730, 1/5000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Rabbit/Mouse IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human Prostate cancer‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human Stromal tumor‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human placenta tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human serous ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human Uterine leiomyoma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human fibroma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • 1/16

    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human aggressive fibromatosis tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    1/16
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Aspartate Aminotransferase Antibody (YA2175) Product Image
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedchemExpress Validation
     Western blot analysis of extracts from A549 (lane 2(20μg)), Hela (lane 3(20μg)), LNcap (lane 4(20μg)), Mouse brain (lane 4(20μg)) and Rat brain (lane 5(20μg)) using Aspartate Aminotransferase Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (beta Actin, HY-P83730, 1/5000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Rabbit/Mouse IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human Prostate cancer‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human Stromal tumor‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human placenta tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human serous ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human Uterine leiomyoma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human fibroma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
    1/1
    MedChemExpress Validation
     Immunohistochemical analysis of paraffin-embedded human aggressive fibromatosis tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Experimental Validation Results for Aspartate Aminotransferase Antibody (YA2175)
  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedchemExpress Validation

    Western blot analysis of extracts from A549 (lane 2(20μg)), Hela (lane 3(20μg)), LNcap (lane 4(20μg)), Mouse brain (lane 4(20μg)) and Rat brain (lane 5(20μg)) using Aspartate Aminotransferase Rabbit mAb. Proteins were transferred to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (beta Actin, HY-P83730, 1/5000) was used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Rabbit/Mouse IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human Prostate cancer‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human Stromal tumor‌ tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human placenta tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human serous ovarian cancer tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human Uterine leiomyoma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human fibroma tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image
    MedChemExpress Validation

    Immunohistochemical analysis of paraffin-embedded human aggressive fibromatosis tissue using Aspartate Aminotransferase antibody was performed. The section was pretreated using high-temperature mediated EDTA antigen retrieval buffer (pH 9.0), for 20 minutes. The tissues were incubated with primary antibody (HY-P82430, 1:200 dilution) at room temperature for 20 minutes. Detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. The tissues were counterstained with hematoxylin and mounted with neutral balsam mounting medium.

  • Aspartate Aminotransferase Antibody (YA2175) Product Image WB
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P
  • Aspartate Aminotransferase Antibody (YA2175) Product Image IHC-P