Anti-VE Cadherin 抗体 - Intercellular Junction Marker (ab33168)

製品の概要

  • 製品名
    Anti-VE Cadherin antibody - Intercellular Junction Marker
    VE Cadherin 一次抗体 製品一覧
  • 製品の詳細
    Rabbit polyclonal to VE Cadherin - Intercellular Junction Marker
  • アプリケーション
    適用あり: ICC/IF, WB, IHC-Fr, IP, In-Cell ELISA, IHC-P, Flow Cytmore details
  • 種交差性
    交差種: Mouse, Chicken, Human
    交差が予測される動物種: Cow, Pig
  • 免疫原

    Synthetic peptide corresponding to Human VE Cadherin aa 750 to the C-terminus conjugated to keyhole limpet haemocyanin.
    (Peptide available as ab27462)

  • ポジティブ・コントロール
    • This antibody gave a positive signal in HUVEC (Human umbilical vein epithelial) Cell Lysate in Western blot, and in confluent HUVEC cells in ICC/IF.

製品の特性

アプリケーション

Our Abpromise guarantee covers the use of ab33168 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

アプリケーション Abreviews 特記事項
ICC/IF Use a concentration of 1 - 5 µg/ml.

Abcam recommends using this product with confluent cells.

WB Use a concentration of 1 µg/ml. Detects a band of approximately 115 kDa (predicted molecular weight: 87 kDa).Can be blocked with VE Cadherin peptide (ab27462).

Abcam recommends using BSA blocking with this product.  Milk blocking will give a greatly reduced signal strength in WB.

IHC-Fr Use at an assay dependent concentration.
IP Use at an assay dependent concentration.
In-Cell ELISA Use at an assay dependent concentration. PubMed: 22689949
IHC-P Use at an assay dependent concentration. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Flow Cyt Use at an assay dependent concentration.

ab171870 - Rabbit polyclonal IgG, is suitable for use as an isotype control with this antibody.

ターゲット情報

  • 機能
    Cadherins are calcium dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. This cadherin may play a important role in endothelial cell biology through control of the cohesion and organization of the intercellular junctions. It associates with alpha-catenin forming a link to the cytoskeleton.
  • 組織特異性
    Endothelial tissues and brain.
  • 配列類似性
    Contains 5 cadherin domains.
  • 翻訳後修飾
    Phosphorylated on tyrosine residues by KDR/VEGFR-2. Dephosphorylated by PTPRB.
  • 細胞内局在
    Cell junction. Cell membrane. Found at cell-cell boundaries and probably at cell-matrix boundaries.
  • Information by UniProt
  • 参照データベース
  • 別名
    • 7B 4 antibody
    • 7B4 antibody
    • 7B4 antigen antibody
    • CADH5_HUMAN antibody
    • Cadherin 5 antibody
    • Cadherin 5 type 2 antibody
    • Cadherin 5, type 2 (vascular endothelium) antibody
    • Cadherin 5, type 2, VE cadherin (vascular epithelium) antibody
    • cadherin, vascular endothelial antibody
    • cadherin, vascular endothelial, 1 antibody
    • Cadherin-5 antibody
    • Cadherin5 antibody
    • CD 144 antibody
    • CD144 antibody
    • CD144 antigen antibody
    • CDH 5 antibody
    • CDH5 antibody
    • CDH5 protein antibody
    • Endothelial specific cadherin antibody
    • FLJ17376 antibody
    • OTTHUMP00000174777 antibody
    • Vascular endothelial cadherin antibody
    • Vascular epithelium cadherin antibody
    • VE Cad antibody
    • VE-cadherin antibody
    • VEC antibody
    see all

Anti-VE Cadherin antibody - Intercellular Junction Marker 画像

  • Anti-VE Cadherin antibody - Intercellular Junction Marker (ab33168) at 1 µg/ml + HUVEC Cell Lysate at 20 µg

    Secondary
    IRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/10000 dilution

    Performed under reducing conditions.

    Predicted band size : 87 kDa
    Observed band size : 115 kDa (why is the actual band size different from the predicted?)
    The band we observe at 115 kDa is believed to be the glycosylated form of the protein.
  • ab33168 stained in HUVEC cells. Cells were fixed with 100% methanol (5min) at room temperature and incubated with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 1h at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab33168 at 1µg/ml and ab7291 (Mouse monoclonal [DM1A] to alpha Tubulin - Loading Control) at 1/1000 dilution overnight at +4°C. The secondary antibodies were ab150120 (pseudo-colored red) and ab150081 (colored green) used at 1 ug/ml for 1hour at room temperature. DAPI was used to stain the cell nuclei (colored blue) at a concentration of 1.43µM for 1hour at room temperature

  • ICC/IF image of VE-Cadherin staining on HUVEC cells using ab33168. The cells were incubated with the primary antibody (ab33168) and the secondary was FITC conjugated anti-rabbit used at 1:400. The cells were incubated with only the secondary antibody as a negative control.
  • ab33168 (1/50) staining VE Cadherin in paraffin-embbeded mouse heart tissue sections. Tissue underwent fixation in formaldehyde, heat-mediated antigen retrieval in citrate buffer and blocking (5 minutes/peroxidase block and 10 minutes/protein block). For further experimental details please refer to abreview.

    See Abreview

  • ab33168 used in Flow cytometry.
    Human REH B cells were fixed in paraformaldehyde and permeabilized using saponin. Primary antibody used undiluted (2µl in 100µl of cells in PBS) and incubated for 15 minutes at 4°C. The secondary antibody used was an undiluted, Alexa Fluor®488 conjugated goat anti-rabbit IgG.

    Rabbit IgG isotype control (white)

    See Abreview

  • ab33168 Immunoprecipitating VE Cadherin in human HUVEC whole cell lysate. 1000000 cells lysate was incubated with primary antibody (1/100 in 0.5% NP40, 150mM NaCl, 50mM Tris) and matrix (Dynabeads) for 2 hours at 4°C. For western blotting a HRP-conjugated mouse anti-VE Cadherin (1/3000) was used to confirm successful immunoprecipation.

    See Abreview

  • ICC/IF image of VE Cadherin stained HUVEC cells. The cells were incubated with the antibody ab33168 at 1/150 (Green). The cells were also stained with Rhodamine phalloidin (Red).

Anti-VE Cadherin antibody - Intercellular Junction Marker (ab33168) 使用論文

This product has been referenced in:
  • Cao Z  et al. The Expression and Functional Significance of Runx2 in Hepatocellular Carcinoma: Its Role in Vasculogenic Mimicry and Epithelial-Mesenchymal Transition. Int J Mol Sci 18:N/A (2017). WB, IF ; Human . Read more (PubMed: 28264434) »
  • Wang M  et al. HIF-1a promoted vasculogenic mimicry formation in hepatocellular carcinoma through LOXL2 up-regulation in hypoxic tumor microenvironment. J Exp Clin Cancer Res 36:60 (2017). WB ; Human . Read more (PubMed: 28449718) »

See all 43 Publications for this product

Product Wall

Abcam guarantees this product to work in the species/application used in this Abreview.
Application
Western blot
Sample
Human Cell lysate - whole cell (human umbilical vein endothelial cell)
Gel Running Conditions
Non-reduced Non-Denaturing (Native) (10%)
Loading amount
20 µg
Treatment
siRNA for 48h
Specification
human umbilical vein endothelial cell
Blocking step
Milk as blocking agent for 10 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: ~25°C
Username

Abcam user community

Verified customer

投稿 Aug 02 2017

Abcam guarantees this product to work in the species/application used in this Abreview.
Application
Immunocytochemistry/ Immunofluorescence
Sample
Mouse Cell (liver)
Permeabilization
Yes - 0.5% TritonX-100
Specification
liver
Blocking step
Serum as blocking agent for 30 minute(s) · Concentration: 5% · Temperature: 37°C
Fixative
Paraformaldehyde
Username

Dr. shuang liang

Verified customer

投稿 Aug 02 2017

Abcam has not validated the combination of species/application used in this Abreview.
Application
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Sample
Hamster Tissue sections (Heart)
Antigen retrieval step
Heat mediated - Buffer/Enzyme Used: Tris EDTA pH 9.0
Permeabilization
No
Specification
Heart
Blocking step
BSA + Milk + Serum as blocking agent for 20 minute(s) · Concentration: 2.0% · Temperature: 27°C
Fixative
Formaldehyde
Username

Dr. Marcelo Pelajo Machado

Verified customer

投稿 Jul 21 2017

Application
Immunocytochemistry/ Immunofluorescence
Sample
Mouse Cell (Primary mouse lung endothelial cells)
Permeabilization
No
Specification
Primary mouse lung endothelial cells
Blocking step
Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 28°C
Fixative
Paraformaldehyde
Username

Dr. Jim Hsiao

Verified customer

投稿 May 01 2017

Abcam guarantees this product to work in the species/application used in this Abreview.
Application
Immunocytochemistry/ Immunofluorescence
Sample
Human Cell (human umbilical vein endothelial cell)
Permeabilization
Yes - 0.5% TritonX-100
Specification
human umbilical vein endothelial cell
Blocking step
Serum as blocking agent for 30 minute(s) · Concentration: 5% · Temperature: 37°C
Fixative
Paraformaldehyde
Username

Dr. shuang liang

Verified customer

投稿 Mar 31 2017

Application
Western blot
Sample
Human Cell lysate - whole cell (human umbilical vein endothelial cell)
Gel Running Conditions
Non-reduced Denaturing (10% gel)
Loading amount
20 µg
Treatment
siRNA for 48hrs
Specification
human umbilical vein endothelial cell
Blocking step
Milk as blocking agent for 10 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: ~25°C
Username

Dr. 振洋 余

Verified customer

投稿 Mar 28 2017

Application
Immunocytochemistry/ Immunofluorescence
Sample
Human Cell (human umbilical vein endothelial cell)
Permeabilization
Yes - 0.5% Triton X-100 for 20min
Specification
human umbilical vein endothelial cell
Blocking step
Serum as blocking agent for 30 minute(s) · Concentration: 5% · Temperature: 37°C
Fixative
Formaldehyde
Username

Dr. 振洋 余

Verified customer

投稿 Mar 24 2017

Abcam guarantees this product to work in the species/application used in this Abreview.
Application
Immunocytochemistry/ Immunofluorescence
Sample
Mouse Cell (Kidney)
Permeabilization
Yes - Low pH Citrate Buffer
Specification
Kidney
Blocking step
BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Fixative
Formaldehyde
Username

Abcam user community

Verified customer

投稿 Feb 02 2017

Abcam has not validated the combination of species/application used in this Abreview.
Application
Immunocytochemistry/ Immunofluorescence
Sample
Rat Cell (primary rat asqtrocytes)
Permeabilization
No
Specification
primary rat asqtrocytes
Blocking step
BSA as blocking agent for 30 minute(s) · Concentration: 3% · Temperature: 23°C
Fixative
Methanol
Username

Lavinia Capuana

Verified customer

投稿 Sep 23 2016

Application
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Sample
Mouse Tissue sections (Kidney)
Antigen retrieval step
Heat mediated - Buffer/Enzyme Used: Tris EDTA pH9.0
Permeabilization
No
Specification
Kidney
Blocking step
BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Fixative
Paraformaldehyde
Username

Abcam user community

Verified customer

投稿 Sep 08 2016

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

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