Parkin Recombinant Rabbit Monoclonal Antibody

货号:
AWA10174
应用:
WB,IHC-P,IF-C,IF-T,FCM,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:

    52 kDa


    Clonality:

    Monoclonal

    Isotype:

    IgG

    Concentration:

    1mg/ml


    Other Names:

    PARK 2; PARK2; PRKN; PRKN2; E3 ubiquitin ligase; E3 ubiquitin-protein ligase parkin; Parkinson juvenile disease protein 2; Parkinson disease protein 2; FRA6E; Park2; Parkin 2; AR JP; LPRS 2; LPRS2; PARK2/Parkin; Parkin; PDJ


    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 1:50-1:200
    IF-C 1:50-1:200
    IF-T 1:50-1:200
    FCM 1:500-1:1000
    IP 1-2ug/sample



    Immunogen

    Information

    Gene Name:

    PRKN

    Protein Name:

    E3 ubiquitin-protein ligase parkin


    Gene ID:

    5071 (Human)  
    50873 (Mouse)  
    56816 (Rat)

    SwissPro:

    O60260 (Human)  
    Q9WVS6 (Mouse)  
    Q9JK66 (Rat)


    Subcellular Location:

    Cytoplasm, cytosol. Nucleus. Endoplasmic reticulum. Mitochondrion. Mitochondrion outer membrane. Cell projection, neuron projection. Postsynaptic density. Presynapse.


    Immunogen:

    Synthetic peptide within N-terminal human Parkin.


    Specificity:

    Parkin Monoclonal Antibody detects endogenous levels of Parkin protein.




    Product images
    Parkin Recombinant Rabbit Monoclonal Antibody - 1 Fig: Immunocytochemistry analysis of HeLa cells labeling Parkin with rabbit anti-Parkin antibody (AWA10147) 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-Parkin antibody (AWA10147) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat anti-Mouse IgG (H+L) Secondary Antibody(Alexa Fluor 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).
    Parkin Recombinant Rabbit Monoclonal Antibody - 2 Fig : Western blot analysis of Parkin 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 ( AWA10174, 1/1000) was used in PBST 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: HUVEC cell
    Lane 3: Hek293T cell
    Lane 4: U251 cell
    Lane 5: GL261 cell
    Lane 6: SH-SY5Y cell
    Lane 7: HT22 cell
    Lane 8: N2A cell
    Lane 9: PC-12 cell
    Lane 10: PC-9 cell
    Lane 11: LLC cell

    Predicted molecular weight: 52 kDa
    Observed molecular weight: 31 kDa
    Exposure time: 45 seconds
    Parkin Recombinant Rabbit Monoclonal Antibody - 3 Fig : Immunohistochemical analysis of paraffin-embedded Rat-cerebellum tissue with Rabbit anti-parkin (AWA10174) 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 (AWA10174) 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
    在线客服
    关闭
    小薇 薇薇 小艾 小奥
    联系销售
    技术支持

    image.png

    月琴艾碧维二维码.jpg