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ISG15 Recombinant Rabbit Monoclonal Antibody

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货号:
AWA22012
应用:
WB,IHC-P,IF-C,FCM
反应性:
Human,Mouse,Rat,Cat
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, Cat

    Molecular Wt:

    Predicted MW: 18 kDa
    Observed MW: 15-17 kDa

     

    Clonality:

    Monoclonal

    Isotype:

    IgG

    Concentration:

    1.125mg/ml

     

    Other Names:

    G1P2; hUCRP; IFI15; IP17; ISG15 ubiquitin like modifier; Ubiquitin like protein ISG15; UCRP; IMD38; ISG15

     

    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 1:1000-1:5000
    IHC-P 1:100-1:500
    IF-C 1:50-1:500
    FCM 1:50-1:200

    Immunogen
    Information

    Gene Name:

    ISG15 G1P2 UCRP

    Protein Name:

    Ubiquitin-like protein ISG15

     

    Gene ID:

    9636 (Human)
    100038882 (Mouse)
    298693 (Rat)

    SwissPro:

    P05161 (Human)      
    Q64339 (Mouse)
    D4A3X3 (Rat)

    Immunogen
    Information

    Subcellular Location:

    Cytoplasm. Secreted.

     

    Immunogen:

    Recombinant fragment of human ISG15.

     

    Specificity:

    ISG15 Monoclonal Antibody detects endogenous levels of ISG15 protein.


    Product images
    ISG15 Recombinant Rabbit Monoclonal Antibody - 1 Fig : Western blot analysis of ISG15 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 (AWA22012, 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: Daudi cell
    Lane 2: A204 cell
    Lane 3: Hela cell
    Lane 4: PC3 cell
    Lane 5: A431 cell
    Lane 6: HepG2 cell
    Lane 7: MDA-MB-231 cell
    Predicted molecular weight:18 kDa
    Observed molecular weight:15-17 kDa
    ISG15 Recombinant Rabbit Monoclonal Antibody - 2 Fig: Immunocytochemistry analysis of RAW264.7 cells(treated with 1 µg/mL LPS for 24h and then treated with 1 µg/mL Brefeldin A for 3h) labeling ISG15 with Rabbit anti-ISG15 antibody(AWA22012)at 1/50 dilution(Green ).
    Cells were fixed in 100% Methanol(-20℃ precool) for 20 minutes , and then blocked with 5% BSA for 60 minutes at 37 ℃. Cells were then incubated with Rabbit anti-ISG15 antibody (AWA22012)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).
    ISG15 Recombinant Rabbit Monoclonal Antibody - 3 Fig:Flow cytometric analysis of HELA cells labeling ISG15.
    Overlay histogram showing HELA cells stained with ISG15 (green line). The cell were fixed in 4% paraformaldehyde for 30 minutes at 37 ℃, permeabilized with 0.02% Triton X-100 in PBS for 30 minutes,and then stained with the primary antibody(AWA22012, 1:50) for 30 min at 4°C. The secondary antibody used was an Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody (AWS0005b) at 1/500 dilution for 30 min at 4ºC. Unlabelled sample was used as a control (cells without incubation with primary antibody; red).
    ISG15 Recombinant Rabbit Monoclonal Antibody - 4 Fig : Immunohistochemical analysis of paraffin-embedded Mouse-brain tissue with Rabbit anti- ISG15 antibody (AWA22012) 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 (AWA22012) 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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