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FITC标记羊抗兔IgG

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  • ¥280
  • 晶风生物
  • TF-8428P
  • 中国
  • 2025年07月13日
  • Elisa=1:500-1000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC=1:100-500,
  • Rabbit
  • Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,Guinea Pig,
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体名

      FITC标记羊抗兔IgG

    • 抗体英文名

      Goat Anti-rabbit IgG/FITC

    • 靶点

      细胞浆 细胞膜 分泌型蛋白

    • 浓度

      1mg/ml

    • 应用范围

      Elisa=1:500-1000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC=1:100-500,

    • 宿主

      Rabbit

    • 适应物种

      Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,Guinea Pig,

    • 保质期

      一年

    • 抗原来源

      Rabbit

    • 目录编号

      TF21166R

    • 级别

      I级

    • 库存

      10

    • 供应商

      晶风生物

    • 标记物

      FITC/Alexa/CY357/BIo/HRP

    • 克隆性

      Polyclonal

    • 保存条件

      -20

    • 形态

      Liquid

    • 亚型

      IgG

    • 免疫原

      KLH conjugated synthetic peptide derived

    • 规格

      100ul

    产品名称:FITC标记羊抗兔IgG
    产品规格:100ul/200ul(部分有50ul,如需更大包装或其他具体规格,请咨询客服)
    研究领域:肿瘤  细胞生物  免疫学等  
    抗体来源:Rabbit
    克隆类型:Polyclonal
    交叉反应:Human,Mouse,Rat,Dog,Pig,Cow,Rabbit,Sheep,
    产品应用:WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1μg/Test IF=1:100-500 (石蜡切片需做抗原修复)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    性    状:Liquid
    浓    度:1mg/ml
    免 疫 原:KLH conjugated synthetic peptide derived 
    亚    型:IgG
    纯化方法:affinity purified by Protein A
    储 存 液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    FITC标记羊抗兔IgG相关抗体示例(非本抗体,如需本抗体,请联系客服索要说明书):
    Sample:
    Liver (Mouse) Lysate at 40 ug
    Spleen (Mouse) Lysate at 40 ug
    NIH/3T3 (Mouse) CellLysate at 30 ug
    RAW246.7 (Mouse) CellLysate at 30 ug
    Primary: Anti- IL12  at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 22 kD
    Observed band size: 35/36 kD
    paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (IL12) Polyclonal Antibody, Unconjugated at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) instructions and DAB staining.
    产品细节图片1
     paraffin embedded (rat brain tissue); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (IL12) Polyclonal Antibody, Unconjugated at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) instructionsand DAB staining.
    产品细节图片2
    FITC标记羊抗兔IgG
    Blank control (blue line): Mouse spleen (blue).
    Primary Antibody (green line): Rabbit Anti- IL12 antibody 
    Dilution: 1μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody (white blue line): Goat anti-rabbit IgG-FITC
    Dilution: 1μg /test.
    Protocol
    The cells were fixed with 70% ice-cold methanol overnight at 4℃. Cells stained with Primary Antibody for 30 min at room temperature. The cells were then incubated in 1 X PBS/2%BSA/10% goat serum to block non-specific protein-protein interactions followed by the antibody for 15 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
    产品细节图片3
    Tissue/cell: rat colitis tissue;  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,at 37℃ for 20 min;
    Incubation: Anti-IL-12 Polyclonal Antibody, Unconjugated 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB staining
    欢迎新老客户咨询订购:FITC标记羊抗兔IgG

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    图标文献和实验
    相关实验
    • 荧光素FITC标记抗体的方法

      FITC在碱性溶液中与抗体蛋白反应时,主要是蛋白质上赖氨酸的r氨基与荧光素的硫碳胺键(thiocarbmide)结合,形成FITC-蛋白质结合物,即荧光抗体或荧光结合物。一个IgG分子中有86个赖氨酸残基,一般最多能结合15~20个,一个IgG分子可结合2~8个分子的FITC,其反应式如下FITC-N=C=S + N-H2-蛋白质 → FITC-NS-C-N-H2-蛋白质常用Marsshall(1958)法标记荧光抗体,也可以根据条件采用Chadwick等标记法或Clark

    • FITC标记抗体-改良法

      ml三蒸水中即成;       方法与步骤:       根据Marshall氏法高效价的抗人球蛋白兔免疫血清,分离球蛋白。       1. 用0.15 mol/L NaCl的盐水及0.15 mol/L pH9.0的NaHCO3-Na2CO3缓冲液稀释使每毫升内含抗体10mg,缓冲液为总量的10%;       2. 将以上溶液降温至4℃,按蛋白:荧光素=50—80mg:1mg的比例加入异硫氰酸荧光素,在0—4℃下电磁搅拌12—14h;       3.用半饱和硫酸铵将标记球蛋白

    • FITC标记抗体-Chadwick氏法

      5.  过柱。取透析过夜的标记物,过葡萄糖凝胶G-25或G-50柱,分离出游离荧光素,收集标记的荧光抗体进行鉴定。

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