EPCAM Recombinant Rabbit Monoclonal Antibody

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货号:
AWA13608
应用:
WB,IHC-P,IF,IP
反应性:
Human,Mouse,Rat
来源:
Rabbit
  • 20μL
  • ¥620
  • 1-3个工作日
  • 50μL
  • ¥1250
  • 1-3个工作日
  • 100μL
  • ¥2200
  • 1-3个工作日
  • 产品概述
  • Product Details

    Host Species:

    Rabbit

    Reactivity:

    Human,Mouse,Rat

    Molecular Wt:

    Predicted MW: 35 kDa
    Observed MW: 40 kDa

     

    Clonality:

    Monoclonal

    Isotype:

    IgG

    Concentration:

    1.185mg/ml

     

    Other Names:

    EGP; CO17 1A; CO 17A; Cell surface glycoprotein Trop-1; ESA; KSA; M4S1; MK-1; DIAR5; EGP-2; EGP40; KS1/4; MIC18; TROP1; BerEp4; EGP314; HNPCC8; LYNCH8; MOC-31; Ber-Ep4; TACSTD1; EpCAM; EPCAM

     

    Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

     

    Purification:

    Affinity-chromatography

     

    Storage:

    Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20°C storage.

    Applications

    WB 1:500-1:2000
    IHC-P 1:100-1:500
    IF 1:50-1:200
    IP 1:100-1:300

    Immunogen
    Information

    Gene Name:

    EPCAM

    Protein Name:

    Epithelial cell adhesion molecule

     

    Gene ID:

    4072 (Human)    
    17075 (Mouse)    
    171577 (Rat)

    SwissPro:

    P16422 (Human)    
    Q99JW5 (Mouse)    
    O55159 (Rat)

    Immunogen
    Information

    Subcellular Location:

    Lateral cell membrane. Cell junction, tight junction.

     

    Immunogen:

    Recombinant fragment of human EPCAM.

     

    Specificity:

    EPCAM Monoclonal Antibody detects endogenous levels of EPCAM protein.


    Product images
    EPCAM Recombinant Rabbit Monoclonal Antibody - 1 Fig : Western blot analysis of EPCAM on different lysates. Proteins were transferred to a NC membrane and blocked with 5% NF-Milk in TBST for 1 hour at room temperature. The primary antibody (AWA13608, 1/1000) was used in TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (AWS0002) at 1:5,000 dilution was used for 1 hour at room temperature.
    Positive control:
    Lane 1: HCT116 cell
    Lane 2: HT-29 cell
    Lane 3: SW620 cell

    Predicted molecular weight:35 kDa
    Observed molecular weight:40 kDa




    EPCAM Recombinant Rabbit Monoclonal Antibody - 2 Fig: Fluorescence immunohistochemical analysis of Rat-ileum tissue (Formalin/PFA-fixed paraffin-embedded sections) with Rabbit anti-EPCAM antibody (AWA13608) at 1/200 dilution.The immunostaining was performed with the TSA Immuno-staining Kit (ABIOWELL, AWI0688). The section was pre-treated using heat mediated antigen retrieval with  Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA13608) at 1/200 dilution for 2 hour at 37℃or overnignt at 4℃. The detection was performed using an HRP conjugated compact polymer system followed by a separate fluorescent tyramide signal amplification system (grenn). DAPI (blue, AWC0291) was used as a nuclear counter stain. Image acquisition was performed with Slide Scanner.

    EPCAM Recombinant Rabbit Monoclonal Antibody - 3 Fig: Immunocytochemistry analysis of HTC-116 cells labeling EPCAM with Rabbit anti-EPCAM antibody (AWA13608) at 1/50 dilution(Green).
    Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.03% Triton X-100 in PBS for 30 minutes, and then blocked with 5% BSA for 60 minutes at 37 ℃. Cells were then incubated with Rabbit anti- EPCAM antibody (AWA13608) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, AWS0005) was used as the secondary antibody at 1/200 dilution for 60 minutes at 37 ℃. Nuclear DNA was labelled in blue with DAPI(AWC0291).

    EPCAM Recombinant Rabbit Monoclonal Antibody - 4 Fig : Immunohistochemical analysis of paraffin-embedded Mouse-bladder tissue with Rabbit anti- EPCAM antibody (AWA13608) at 1/200 dilution.
    The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA13608) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system(ABIOWELL, AWI0629). DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

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