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Donkey Anti-Goat IgG H&L (Biotin)

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1mg
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产品详情
  • 产品名称

    驴抗山羊IgG H&L (Biotin)
    参阅全部 IgG 二抗

  • 宿主

    Donkey

  • 靶标种属

    Goat

  • 经测试应用

    适用于: ICC/IFDot blotELISAIHC-PIHC-FrImmunomicroscopyWBmore details

  • 免疫原

    Full length native Goat IgG (purified).

  • 偶联物

    Biotin

  • 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

    Preservative: 0.01% Sodium azide
    Constituents: 1% BSA, 0.424% Potassium phosphate solution, 0.88% Sodium chloride

  • 纯度

    Affinity purified

  • 纯化说明

    This product was prepared from monospecific antiserum by immunoaffinity chromatography using Goat IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities.

  • 克隆

    多克隆

  • 同种型

    IgG

  • 常规说明

    Use donkey anti-goat IgG (H&L) biotin to confidently detect primary antibodies raised in goat in your immunohistochemistry, western blot, ELISA or immunoprecipitation. Get dilutions to get the best results in your IHC, WB, IP, or ELISA with donkey anti-goat IgG (H&L) biotin below. 

     

    Conjugation notes

    Biotinamidocaproate N-Hydroxysuccinimide Ester (BAC) Biotin/Protein Ratio: 10-20 BAC molecules per IgG molecule

The Abpromise guarantee

Abpromise™承诺保证使用ab6884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/IF

1/1000 - 1/5000.

Dot blot

Use at an assay dependent dilution.

ELISA

1/180000.

IHC-P

Use at an assay dependent dilution.

IHC-Fr

Use at an assay dependent dilution.

Immunomicroscopy

Use at an assay dependent dilution.

WB

1/2000 - 1/10000.

  • Immunohistochemistry (Frozen sections) - Donkey Anti-Goat IgG H&L (Biotin) (ab6884)

    Immunohistochemistry (Frozen sections) - Donkey Anti-Goat IgG H&L (Biotin) (ab6884)Image from Dr WZ Wang et al, BMC Mol Biol. 2009 Jul 6;10:69, Fig 2.

    ab6884 used to stain samples of whole heads of embryonic day 15 (E15) mice by Immunohistochemistry (Formalin-fixed, paraffin-embedded sections).
    Comparison of four staining methods. The heads were flash-frozen directly in isopentane on dry-ice. Once hardened, they were embedded in O.C.T compound. Frozen sections were postfixed in 4% paraformaldehyde in PBS for 20 minutes and quenched in 1.5% hydrogen peroxide for 30 minutes. Sections were then blocked for 2 hours at room temperature with 5% donkey serum in Tris-buffered saline with 0.1% Triton-X100 and then incubated with a goat anti-Nurr1 primary antibody 1/200 in 1% donkey serum in TBS at 4°C overnight. Biotinylated donkey anti-goat (ab6884) 1/500 in 1% donkey serum in TBS was applied for 2 hours at room temperature and reacted with avidin-biotinylated enzyme complex (ABC) using the Vectastain Elite kit and diaminobenzidene (DAB) according to the manufacturer's instructions. Images were taken directly on the PALM Micr