pro Caspase-7 Recombinant Rabbit Monoclonal Antibody

货号:
AWA12689
应用:
WB,IHC-P,IF
反应性:
Human
来源:
Rabbit
  • 20μL 
  • ¥620
  • 有库存
  • 50μL 
  • ¥1250
  • 有库存
  • 100μL 
  • ¥2200
  • 有库存
  • 产品概述
  • Product Details

     

    Host Species:

    Rabbit

    Reactivity:

    Human

    Molecular Wt:

    34 kDa


    Clonality:

    Monoclonal

    Isotype:

    IgG

    Concentration:

    1 mg/ml


    Other Names:

    CASP7; MCH3; Caspase-7; CASP-7; Apoptotic protease Mch-3; CMH-1; ICE-like apoptotic protease 3; ICE-LAP3; proCaspase-7; proCaspase7

     


    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 1:1000-1:2000

    IHC-P 1:50-1:200

    IF 1:50-1:200

     



    Immunogen Information

    Gene Name:

    CASP7

    Protein Name:

    Caspase7


    Gene ID:

    840 (Human)     

    12369 (Mouse)     

     

    SwissPro:

    P55210 (Human)     

    P97864 (Mouse)     

     


    Immunogen:

    Synthetic peptide within Human Caspase 7 AA range: 1-50.


    Specificity:

    pro Caspase-7 Monoclonal Antibody detects endogenous levels of pro Caspase-7 protein.

     




    Product images
    pro Caspase-7 Recombinant Rabbit   Monoclonal Antibody - 1 Fig : Western blot analysis of pro caspase 7 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 (AWA12689, 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: 4T1 cell
    Lane 2: SHZ-88 cell
    Lane 3: HEPA1-6 cell
    Lane 4: HELA cell
    Lane 5: HEK-293 cell
    Lane 6: HEPG2 cell
    Lane 7: NIH3T3 cell
    pro Caspase-7 Recombinant Rabbit   Monoclonal Antibody - 2 Fig: Immunocytochemistry analysis of HeLa cells labeling pro-caspase7 with rabbit anti-pro-caspase7 antibody ( AWA12689) at 1/50 dilution(red).

    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-pro-caspase7 antibody ( AWA12689) 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).
    pro Caspase-7 Recombinant Rabbit   Monoclonal Antibody - 3 Fig : Immunohistochemical analysis of paraffin-embedded mouse-kidney tissue with rabbit anti-pro-caspase7 antibody ( AWA12689 ) 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 (AWA12689) 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.
    pro Caspase-7 Recombinant Rabbit   Monoclonal Antibody - 4 Fig : Immunohistochemical analysis of paraffin-embedded rat-kidney tissue with rabbit anti-pro-caspase7 antibody ( AWA12689 ) 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 (AWA12689) 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.
    细胞描述: GH3细胞系是由Tashjian AH等在1965年7月从一只7月龄的雌性Wistar-Furth大鼠的垂体肿瘤中分离建立的。GH3细胞系不是直接来源于GH1细胞系的克隆,而是从原代培养的GH1细胞在大鼠身上传代两次形成的肿瘤中建立的。上皮样的GH3细胞比GH1分泌更高水平的生长激素,也可产生
    细胞描述: GH3细胞系是由Tashjian AH等在1965年7月从一只7月龄的雌性Wistar-Furth大鼠的垂体肿瘤中分离建立的。GH3细胞系不是直接来源于GH1细胞系的克隆,而是从原代培养的GH1细胞在大鼠身上传代两次形成的肿瘤中建立的。上皮样的GH3细胞比GH1分泌更高水平的生长激素,也可产生
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