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Anti-LYVE1 antibody

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  • 产品名称

    Anti-LYVE1抗体
    参阅全部 LYVE1 一抗

  • 描述

    兔多克隆抗体to LYVE1

  • 宿主

    Rabbit

  • 经测试应用

    适用于: IHC-FrFlow CytIHC-PWBmore details

  • 种属反应性

    与反应: Human
    预测可用于: Rat

  • 免疫原

    Recombinant fragment corresponding to Human LYVE1 aa 1-250. Recombinant human soluble LYVE1 fragment produced in insect cells (ab54341).
    Database link: 
    Q9Y5Y7

  • 阳性对照

    • human colon carcinoma

  • 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. Avoid freeze / thaw cycle.

  • 存储溶液

    Constituent: PBS

  • 浓度

    • 100 µg 浓度为 1 mg/ml

  • 纯度

    Protein A purified

  • 纯化说明

    Protein-A Chromatography (+his tag depleted).

  • Primary antibody说明

    The lymphatic vasculature forms a second circulatory system that drains extracellular fluid from the tissues and provides an exclusive environment in which immune cells can encounter and respond to foreign antigen. Recently a number of interesting molecules have been identified that may be exploited as markers for lymphatic endothelium, including the hyaluronan receptor LYVE1, PALE, VEGFR3, podoplanin.

  • 克隆

    多克隆

  • 同种型

    IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab10278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
IHC-Fr(1)

Use a concentration of 6 - 30 µg/ml. 

Fix sections for 10 min at -20°C in MeOH.

Flow Cyt(1)

Use at an assay dependent concentration.

IHC-P(2)

Use a concentration of 2 µg/ml.

WB

Use a concentration of 1 - 2 µg/ml. Detects a band of approximately 35-45 kDa (predicted molecular weight: 35 kDa).

  • 数据库链接

  • 别名

    • CRSBP1 antibody

    • extracellular link domain containing 1 antibody

    • extracellular link domain-containing 1 antibody

    • Extracellular link domain-containing protein 1 antibody

    • HAR antibody

    • Hyaluronic acid receptor antibody

    • Lymphatic endothelium specific hyaluronan receptor antibody

    • lymphatic vessel endothelial hyaluronan receptor 1 antibody

    • Lymphatic vessel endothelial hyaluronic acid receptor 1 antibody

    • LYVE 1 antibody

    • LYVE-1 antibody

    • LYVE1 antibody

    • LYVE1_HUMAN antibody

    • XLKD1 antibody

    • Cell surface retention sequence-binding protein 1 antibody

    • CRSBP 1 antibody

    • CRSBP-1 antibody

  • Immunohistochemistry (Frozen sections) - Anti-LYVE1 antibody (ab10278)

    Immunohistochemistry (Frozen sections) - Anti-LYVE1 antibody (ab10278)

    Immunohistochemistry (Frozen sections) analysis of human colon carcinoma tissue sections labelling LYVE1 with ab10278.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LYVE1 antibody (ab10278)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-LYVE1 antibody (ab10278)

    ab10278 (2µg/ml) staining LYVE1 in human colon using an automated system (DAKO Autostainer Plus). Using this protocol there is lymphatic endothelium staining of lymphatic ducts where blood vessel endothelium and smooth muscle is wholly negative.
    Sections were rehydrated and antigen retrieved with the Dako 3-in-1 AR buffer citrate pH 6.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.

  • Western blot - Anti-LYVE1 antibody (ab10278)

    Western blot - Anti-LYVE1 antibody (ab10278)

    All lanes : Anti-LYVE1 antibody (ab10278) at 1 µg/ml

    Lane 1 : A549 (Human lung adenocarcinoma epithelial cell line) Whole Cell Lysate
    Lane 2 : HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate

    Lysates/proteins at 10 µg per lane.

    Secondary
    All lanes : Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 35 kDa
    Observed band size: 37 kDa
    why is the actual band size different from the predicted?
    Additional bands at: 22 kDa, 55 kDa. We are unsure as to the identity of these extra bands.


    Exposure time: 4 minutes


    LYVE-1 contains a number of potential glycosylation sites (SwissProt) which may explain its migration at a higher molecular weight than predicted.

  • Flow Cytometry - Anti-LYVE1 antibody (ab10278)

    Flow Cytometry - Anti-LYVE1 antibody (ab10278)

    Flow Cytometry analysis of human dermal microvascular endothelial cells (HDMVEC) labelling LYVE1 with ab10278.

  • Western blot - Anti-LYVE1 antibody (ab10278)

    Western blot - Anti-LYVE1 antibody (ab10278)

    All lanes : Anti-LYVE1 antibody (ab10278)

    Lane 1 : Recombinant Human LYVE1 protein (
    ab54341)
    Lane 2 : Recombinant Mouse LYVE1 protein (
    ab54342)

    Predicted band size: 35 kDa

  • Immunohistochemistry (Frozen sections) - Anti-LYVE1 antibody (ab10278)

    Immunohistochemistry (Frozen sections) - Anti-LYVE1 antibody (ab10278)This image is courtesy of an Abreview submitted by Dr Vyacheslav Ogay

    Rat skin was fixed with paraformaldehyde in 15% saturated picric acid solution for 4hr. Prior to sectioning, the specimen was infiltrated in O.C.T. and frozen in isopentane. The frozen specimen was sectioned these were rinsed in PBS for 15 min to remove O.C.T. and incubated in a 3% sodium deoxycholate solution. The specimens were rinsed twice with distilled water and then with PBS three times. The sections were incubated in 10% normal goat serum for 12 hr at 4°C, then for 12 hr with ab10278. After washing with PBS, the specimens were incubated with Alexa Fluor® 555-conjugated goat anti-rabbit IgG (H+L) (1:500),  for 12 hr at 4°C. The cell nuclei were counterstained with YoYo-1. Images were obtained by using confocal microscope.

    See Abreview