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Anti-VEGF Receptor 2 (phospho Y1054 + Y1059) antibody

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50uL
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  • 产品名称

    Anti-VEGF Receptor 2 (phospho Y1054 + Y1059)抗体
    参阅全部 VEGF Receptor 2 一抗

  • 描述

    兔多克隆抗体to VEGF Receptor 2 (phospho Y1054 + Y1059)

  • 宿主

    Rabbit

  • 经测试应用

    适用于: ICCWBmore details

  • 种属反应性

    与反应: Human
    预测可用于: Mouse, Rat

  • 免疫原

    Synthetic peptide corresponding to Human VEGF Receptor 2 (phospho Y1054 + Y1059).

  • 阳性对照

    • ICC: VEGF treated HUVEC whole cells. WB: VEGF treated HUVEC, MDA-MB-231 and MCF7 whole cell extract.

  • 常规说明


    The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.

    If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As

  • 形式

    Liquid

  • 存放说明

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

  • 存储溶液

    pH: 7.30
    Preservative: 0.05% Sodium azide
    Constituents: PBS, 0.1% BSA, 50% Glycerol

  • 纯度

    Immunogen affinity purified

  • 纯化说明

    The antibody has been negatively preadsorbed using a non-phosphopeptide corresponding to the site of phosphorylation to remove antibody that is reactive with non-phosphorylated VEGFR 2. The final product is generated by affinity chromatography using a VEGFR 2 derived peptide that is phosphorylated at Tyrosines 1054 and 1059.

  • 克隆

    多克隆

  • 同种型

    IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab5473于以下的经测试应用

“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。

应用Ab评论说明
ICC

1/250.

WB(1)

1/1000. Detects a band of approximately 150 kDa.

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  • Immunocytochemistry - Anti-VEGF Receptor 2 (phospho Y1054 + Y1059) antibody (ab5473)

    Immunocytochemistry - Anti-VEGF Receptor 2 (phospho Y1054 + Y1059) antibody (ab5473)

    Immunofluorescence analysis of HUVEC cells labelling VEGF Receptor 2 (phospho Y1054 + Y1059) (PAnel a: green) using ab5473 at 2 ug/ml in 0.1% BSA for 3 hours at room temperature, follwed by Alexa Fluor® 488-conjugated Goat anti-rabbit IgG polyclonal at 1/2000 dilution. Pbel b: Nuclei stained with DAPI (blue), Panel c: F-actin stained with Alexa Fluor® 555 Rhodamine Phalloidin (red), Panel d: Merged images. The images were captured at 60X magnification.

    Prior antibody incubation, HUVEC (Human umbilical vein endothelial cell line) cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.1% Triton™ X-100 for 10 minutes and blocked with 1% BSA for 1 hour at room temperature, followed by treatment with 100 ng of VEGF for 30 minutes. Assay was done on 90% confluent log phase HUVEC cells.

     

  • Western blot - Anti-VEGF Receptor 2 (phospho Y1054 + Y1059) antibody (ab5473)

    Western blot - Anti-VEGF Receptor 2 (phospho Y1054 + Y1059) antibody (ab5473)

    All lanes : Anti-VEGF Receptor 2 (phospho Y1054 + Y1059) antibody (ab5473) at 1/1000 dilution

    Lane 1 : HUVEC (Human umbilical vein endothelial cell line) whole cell extract with Skimmed milk
    Lane 2 : HUVEC cells treated with 25ng/ml VEGF for 5 minutes with Skimmed milk
    Lane 3 : MDA-MB-231 (human breast adenocarcinoma cell line) whole cell extract with Skimmed milk
    Lane 4 : MCF7 (human breast adenocarcinoma cell line) whole cell extract with Skimmed milk

    Lysates/proteins at 30 µg per lane.

    Blocking peptides at 5 % per lane.

    Secondary
    All lanes : Goat anti-rabbit IgG HRP conjugate at 1/5000 dilution


    A 150 kDa band corresponding to VEGFR (pYpY1054/1059) was observed across cell lines tested.

    Protein samples were electrophoresed using Novex® NuPAGE® 10 % Bis-Tris gel, XCell SureLock™ Electrophoresis System and Novex® Sharp Pre-Stained Protein Standard.

    Resolved proteins were then transferred onto a nitrocellulose membrane by over night wet transfer. 

    Chemiluminescent detection was performed using Pierce™ ECL Western Blotting Substrate.