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山羊 anti-大鼠 IgG2b Antibody (TRITC)

ELISA, IHC, IF, ICC Polyclonal TRITC
产品编号 ABIN1099730
发货至: 中国
  • 抗原 See all IgG2b products
    IgG2b
    适用
    • 81
    • 22
    大鼠
    宿主
    • 58
    • 25
    • 12
    • 7
    • 1
    山羊
    克隆类型
    • 70
    • 19
    多克隆
    标记
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    TRITC
    应用范围
    • 46
    • 45
    • 32
    • 30
    • 25
    • 21
    • 7
    • 5
    • 5
    • 5
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    ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunocytochemistry (ICC)
    特异性
    The reactivity of the antiserum is directed to the subclass IgG2b.
    产品特性
    Physicochemical characteristics: IgG protein concentration 10 mg/mL. Fluorochrome/IgG protein molar ratio (F/P) is approximately 1.8.

    Physical form: TRITC-coupled purified hyperimmune goat IgG lyophilized from a solution in phosphate buffered saline (PBS, pH 7.2).

    Fluorescent marker: Tetramethylrhodamine isothiocyanate isomer R. It has an orange-red fluorescence.
    Excitation: 554 nm, emission: 573 nm. To avoid nonspecific background staining, specially synthesized and exceptionally pure crystalline isomer R has been used instead of the usual racemic mixture. Although its fluorescence efficiency is less than of FITC, TRITC conjugates have the advantage of significantly less photo bleaching. This facilitates their use in quantitative cell-counting procedures.

    Conjugation procedure: A proprietary technique for the binding of TRITC is used, followed by several purification steps to remove free reactants and protein aggregates. After each step activity and specificity are tested in a variety of techniques. The conjugate is lyophilized to assure stability and long shelf life.
    纯化方法
    Hyperimmune antisera with strong precipitating activity are selected for fractionation and purification of the IgG (7S) fraction containing the bulk of the defined antibody specificity. It is free of other serum proteins as tested by immunoelectrophoresis.
    Adsorption: Immunoaffinity adsorbed using insolubilized antigens as required to eliminate antibodies cross-reacting with other components of the immunoglobulin system or reacting with other serum proteins. Special attention is given to the removal of antibodies to common Ig/Fab. The use of insolubilized adsorption antigens prevents the presence of excess adsorbent protein or immune complexes in the antiserum.
    免疫原
    Pools of purified homogenous IgG2b isolated from rat serum. Freund's complete adjuvant is used in the first step of the immunization procedure.
  • 应用备注
    Working dilutions are usually between 1:10 and 1:60, depending on the method used.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    It is reconstituted by adding 1 mL sterile distilled water, spun down to remove insoluble particles, divided into small aliquots, frozen and stored at or below -20 °C.
    缓冲液
    Phosphate buffered saline (PBS, pH 7.2)
    储存液
    Without preservative
    注意事项
    Prior to use, an aliquot is thawed slowly at ambient temperature, spun down again and used to prepare working dilutions by adding sterile phosphate buffered saline (PBS, pH 7.2). Repeated thawing and freezing should be avoided. Working dilutions should be stored at +0 °C, not refrozen, and preferably used the same day. If a slight precipitation occurs upon storage, this should be removed by centrifugation. It will not affect the performance of the immunoconjugate.
    储存条件
    4 °C/-20 °C
    储存方法
    The lyophilized conjugate is shipped at ambient temperature and may be stored at +4 °C, prolonged storage at or below -24 °C.
  • 抗原
    IgG2b
    Abstract
    IgG2b 产品
    物质类
    Antibody
    背景
    In immunocytochemical and immunohistochemical staining for the detection of IgG2b at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates, to identify and measure IgG2b in rat serum or other body fluids. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal.
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