NR2F1 Recombinant Rabbit Monoclonal Antibody

货号:
AWA10544
应用:
WB,IHC-P
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:

    46 kDa


    Clonality:

    Monoclonal

    Isotype:

    IgG

    Concentration:

    1 mg/ml


    Other Names:

    COUP TF I; COUP TF1; COUP TFI; COUP transcription factor 1; COUP transcription factor I; EAR 3; EAR3; ERBAL3; NR2F1; NR2F2; SVP44; TCFCOUP1; TFCOUP1; V erbA related protein 3

     


    Formulation:

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


    Purification:

    Affinity-chromatography


    Storage:

    -20°C,1 year



    Applications

     

    WB 1:1000

    IHC-P 1:1000



    Immunogen

    Information

    Gene Name:

    NR2F1 

    Protein Name:

    COUP transcription factor 1


    Gene ID:

    7025 (Human)     

    13865 (Mouse)     

    81808 (Rat)

    SwissPro:

    P10589 (Human)     

    Q60632 (Mouse)     

    Q62681 (Rat)

     


    Subcellular Location:

    Nucleus.


    Immunogen:

    Synthetic peptide within Human NR2F1. AA range: 1-50.


    Specificity:

    NR2F1 Monoclonal Antibody detects endogenous levels of NR2F1 protein.




    Product images
    NR2F1 Recombinant Rabbit Monoclonal Antibody - 1 Fig: Fluorescence immunohistochemical analysis of Mouse-cerebellum tissue (Formalin/PFA-fixed paraffin-embedded sections). with Rabbit anti-NR2F1 antibody (AWA10544) 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 (AWA10544) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system followed by a separate fluorescent tyramide signal amplification system (green). DAPI (blue, AWC0291) was used as a nuclear counter stain. Image acquisition was performed with Slide Scanner.
    NR2F1 Recombinant Rabbit Monoclonal Antibody - 2 Fig : Immunohistochemical analysis of paraffin-embedded Rat-brain tissue with Rabbit anti-NR2F1 antibody (AWA10544) 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 (AWA10544) at 1/200 dilution for 2 hour at 37℃or overnignt at 4℃. 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.
    NR2F1 Recombinant Rabbit Monoclonal Antibody - 3 Fig : Western blot analysis of NR2F1 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 (AWA10544, 1/2000) 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: Rat brain
    Lane 2: PC12 cell
    Lane 3: Hela cell
    Lane 4: NIH3T3 cell

    Predicted molecular weight:46 kDa
    Observed molecular weight:44 kDa;

    Exposure time: 90 seconds
    NR2F1 Recombinant Rabbit Monoclonal Antibody - 4 Fig: Fluorescence immunohistochemical analysis of Mouse-retina tissue (Formalin/PFA-fixed paraffin-embedded sections). with Rabbit anti-NR2F1 antibody (AWA10544) 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 (AWA10544) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system followed by a separate fluorescent tyramide signal amplification system (green). DAPI (blue, AWC0291) was used as a nuclear counter stain. Image acquisition was performed with Slide Scanner.
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