订购/客服:021-61998551/13122364865

Anti-Integrin Alpha V + Beta 3 (CD51+CD61) antibody

Anti-Integrin Alpha V + Beta 3 (CD51+CD61) antibody
别名: Integrin Alpha V + Beta 3 (CD51+CD61)
适用物种: Human,Mouse,Rat  
验证应用: WB,IHC-P,FC  
种属: 兔多抗  
储存条件: -20℃ 
Anti-Integrin Alpha V + Beta 3 (CD51+CD61) antibody
货号 规格 可用库存 销售价(RMB) 您的折扣价(RMB) 购买数量
ZY6911-52R-50 μl 兔多抗 现货 1500.00 1500
ZY6911-52R-100 μl 兔多抗 现货 2500.00 2500
熔点:
密度:
储存条件: -20℃

 

Anti-Integrin Alpha V + Beta 3 (CD51+CD61) antibody

 

  • 概述

  • 产品名称Anti-Integrin Alpha V + Beta 3 (CD51+CD61) antibody

  • 分子量KDa

  • 种属反应性Human,Mouse,Rat

  • 验证应用WB,IHC-P,FC

  • 抗体类型兔多抗

  • 免疫原KLH conjugated synthetic peptide derived from human Integrin Alpha V + Beta 3

  • 偶联Non-conjugated

  • 性能

  • 形态Liquid

  • 浓度1 mg/mL.

  • 存放说明Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20℃. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4℃.

  • 存储缓冲液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

  • 亚型IgG

  • 纯化方式affinity purified by Protein A

  • 亚细胞定位Cell Membrane; single-pass type I membrane protein.

  •  

  • ​其它名称CD51 + CD61
    CD51
    CD61
    GP3A
    GPIIIa
    integrin alpha v
    integrin beta 3
    intregrin alpha v beta 3
    ITGAV
    ITGB3
    Platelet membrane glycoprotein IIIa
    Vitronectin receptor alpha subunit
    VNRA
    Antigen identified by monoclonal antibody L230
    CD51 antigen
    CD61 antigen
    DKFZp686A08142
    Integrin alpha V (vitronectin receptor, alpha polypeptide, antigen CD51)
    integrin alpha v
    Integrin beta 3 (platelet glycoprotein IIIa, antigen CD61)
    Integrin beta chain beta 3
    intregrin alpha v beta 3
    ITGAV
    MSK8
    Platelet glycoprotein IIIa
    Platelet membrane glycoprotein IIIa
    Vitronectin receptor alpha subunit
    Vitronectin receptor subunit alpha.

    more
  • 应用

    WB:1:500-2000
    IHC-P:1:400-800
    FC:1μg/Test

  •  

    Fig1: Tissue/cell: rat brain tissue; 4% Paraformaldehyde-fixed and paraffin-embedded;
    Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
    Incubation: Anti-Integrin Alpha V + Beta 3(CD51+CD61) Polyclonal Antibody, Unconjugated 1:200, overnight at 4℃, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining

     

    Fig2: cell: mouse lung.
    Incubation: Avoid light, at 4℃ for 40 minutes. Red line: Blank control (mouse lung cells),2X10^6/ml, at 4℃ for 40 minutes. Green line: (primary antibody) Integrin Alpha V + Beta 3 (CD51+CD61) (bs-1310R), (secondary antibody)Goat Anti-rabbit IgG/FITC (bs-0295G-FITC), 1:00, at 4℃ for 40 minutes.

     

    Fig3: Cell: MCF-7
    Concentration:1:100
    Host/Isotype:Rabbit/IgG
    Flow cytometric analysis of Rabbit IgG isotype control on MCF-7(green) compared with control in the absence of primary antibody (blue) followed by Alexa Fluor 488-conjugated goat anti-rabbit IgG(H+L) secondary antibody .

     

    Fig4: Blank control: U937(blue).
    Primary Antibody: Rabbit Anti-Integrin Alpha V + Beta 3 (CD51+CD61) antibody Dilution: 1μg in 100 μL 1X PBS containing 0.5% BSA;
    Isotype Control Antibody: Rabbit IgG(orange) ,used under the same conditions );
    Secondary Antibody: Goat anti-rabbit IgG-PE(white blue), Dilution: 1:200 in 1 X PBS containing 0.5% BSA.
    Protocol
    The cells were fixed with 2% paraformaldehyde (10 min). Primary antibody (, 1μg /1x10^6 cells) were incubated for 30 min on the ice, followed by 1 X PBS containing 0.5% BSA + 10% goat serum (15 min) to block non-specific protein-protein interactions. Then the Goat Anti-rabbit IgG/PE antibody was added into the blocking buffer mentioned above to react with the primary antibody at 1/200 dilution for 30 min on ice. Acquisition of 20,000 events was performed.

     

    Fig5: Tissue/cell: Human lung cancer tissue; 4% Paraformaldehyde-fixed and paraffin-embedded;
    Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
    Incubation: Anti-Integrin Alpha V + Beta 3 (CD51 + CD61) Polyclonal Antibody, Unconjugated 1:200, overnight at 4℃, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining

     

    Fig6: Tissue/cell: Human laryngeal tissue; 4% Paraformaldehyde-fixed and paraffin-embedded;
    Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
    Incubation: Anti-Integrin Alpha V + Beta 3 (CD51 + CD61) Polyclonal Antibody, Unconjugated1:200, overnight at 4℃, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining

     

    Fig7: Sample: HUVEC (human)Cell Lysate at 40 ug
    Primary: Anti- Integrin Alpha V + Beta 3 (CD51+CD61) at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 116 kD
    Observed band size: 120 k

  •  

特别提示:本公司的所有产品仅可用于科研实验,严禁用于临床医疗及其他非科研用途!

  • 专业包装 正品保证

  • 快乐服务 售后无忧

  • 会员特权 优惠不断

  • 个人信息 严格保护


© 2005-2024 泽叶生物网站 版权所有,并保留所有权利。
沪ICP备16043273号-2号