Cleaved Caspase-9 p10(D330) Rabbit Polyclonal Antibody

货号:
AWA46474
应用:
WB,IHC,IF,ELISA
反应性:
Human,Mouse,Rat
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,Mouse,Rat

    Molecular Wt:

    10,46 kDa


    Clonality:

    Polyclonal

    Isotype:

    IgG

    Concentration:

    1 mg/ml


    Other Names:

    CASP9; MCH6; Caspase-9; CASP-9; Apoptotic protease Mch-6; Apoptotic protease-activating factor 3; APAF-3; ICE-like apoptotic protease 6; ICE-LAP6

     


    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 1:500-1:2000

    IHC 1:100-1:300

    IF 1:50-1:200

    ELISA 1:20000

    Not yet tested in other applications.

     



    Immunogen

    Information

    Gene Name:

    CASP9 

    Protein Name:

    Caspase-9


    Gene ID:

    842 (Human)     

    12371 (Mouse)     

    58918 (Rat)

    SwissPro:

    P55211 (Human)     

    Q8C3Q9 (Mouse)     

    Q9JHK1 (Rat)

     


    Subcellular Location:

    Nucleus, mitochondrion, cytosol, apoptosome.


    Immunogen:

    The antiserum was produced against synthesized peptide derived from human Caspase 9. AA range: 281-330.

     


    Specificity:

    Cleaved Caspase-9 p10 (D330) Polyclonal Antibody detects endogenous levels of fragment of activated Caspase-9 p10 protein resulting from cleavage adjacent to D330.

     




    Product images
    Cleaved Caspase-9 p10(D330) Rabbit Polyclonal Antibody - 1 Fig : Western blot analysis of Cleaved caspase9 p10 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 (AWA46474, 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: Hela cell
    Lane 2: Jurkat cell
    Lane 3: THP-1 cell
    Lane 4: Rat brain
    Lane 5: HL-60 cell
    Lane 6: NIH3T3 cell
    Lane 7: HepG2 cell

    Exposure time: 15 seconds
    Predicted molecular weight:10/46 kDa
    Observed molecular weight:52KD(Full length caspase9)、35/37/17/12 KDa(Cleaved caspase9);
    Cleaved Caspase-9 p10(D330) Rabbit Polyclonal Antibody - 2 Fig : Western blot analysis of Cleaved Caspase9 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 (AWA46474, 1/1000) was used in TBST at room temperature for 2 hours. Goat Anti-Ribbit IgG - HRP Secondary Antibody (AWS0002) at 1:5,000 dilution was used for 1 hour at room temperature.
    Positive control:
    Lane 1: 3D4/21 cell
    Lane 2: 3D4/21 cell treated with 800 μmH2O2 for 24 hours
    Lane 3:Hela cell
    Lane 4:Hela cell treated with 1μM staurosporine for 24 hours

    Predicted molecular weight:46/35KD
    Observed molecular weight:51/38KD;

    Exposure time: 7seconds
    Cleaved Caspase-9 p10(D330) Rabbit Polyclonal Antibody - 3 Fig : Immunohistochemical analysis of paraffin-embedded Rat-brain tissue with Rabbit anti-Caspase 9 antibody (AWA46474) 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 (AWA46474) 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.
    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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