Invitrogen A-11029 Goat anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor™ 488
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Invitrogen A-11029 Goat anti-M

ouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor™ 488
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  • ¥3838
  • Invitrogen
  • A-11029
  • 美国
  • 2025年12月14日
  • 免疫细胞化学 / 免疫荧光(ICC/IF),,免疫组织化学(IHC)流式细胞分析(Flow),
  • 山羊
  • 小鼠
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  • 企业认证

    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体名

      羊抗小鼠 IgG(H+L)高度交叉吸附二抗,Alexa Fluor™ 488 标记

    • 抗体英文名

      Goat anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor™ 488

    • 靶点

      小鼠 IgG 分子的重链(Heavy chain)和轻链(Light chain

    • 浓度

      2 mg/mL

    • 应用范围

      免疫细胞化学 / 免疫荧光(ICC/IF),,免疫组织化学(IHC)流式细胞分析(Flow),

    • 宿主

      山羊

    • 供应商

      上海然其生物科技有限公司

    • 库存

      现货

    • 级别

      见包装

    • 目录编号

    • 抗原来源

      小鼠 IgG 的重链和轻链

    • 保质期

      见包装

    • 适应物种

      小鼠

    • 标记物

      偶联 Alexa Fluor™ 488 荧光染料,其激发波长约为 499nm,发射波长约为 520nm,适配 488nm 激光通道。

    • 克隆性

      多克隆

    • 保存条件

      4℃避光保存,严禁冷冻,避免反复冻融

    • 形态

      液体

    • 亚型

      IgG

    • 免疫原

      小鼠 IgG(免疫球蛋白 G)的重链和轻链完整分子。

    • 规格

      1mg

    产品详细信息

    To minimize cross-reactivity, the goat anti-mouse IgG whole antibodies have been highly cross-adsorbed against bovine IgG, goat IgG, rabbit IgG, rat IgG, human IgG, and human serum. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in higher sensitivity and less background staining. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only the nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. Further passages through additional columns result in 'highly cross-adsorbed' preparations of secondary antibody. The benefits of these extra steps are apparent in multiplexing/multicolor-staining experiments where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there may be the presence of endogenous immunoglobulins.

    Alexa Fluor dyes are among the most trusted fluorescent dyes available today. Invitrogen™ Alexa Fluor 488 dye is a bright, green-fluorescent dye with excitation ideally suited to the 488 nm laser line. For stable signal generation in imaging and flow cytometry, Alexa Fluor 488 dye is pH-insensitive over a wide molar range. Probes with high fluorescence quantum yield and high photostability allow detection of low-abundance biological structures with great sensitivity. Alexa Fluor 488 dye molecules can be attached to proteins at high molar ratios without significant self-quenching, enabling brighter conjugates and more sensitive detection. The degree of labeling for each conjugate is typically 2-8 fluorophore molecules per IgG molecule; the exact degree of labeling is indicated on the certificate of analysis for each product lot.

    Using conjugate solutions: Centrifuge the protein conjugate solution briefly in a microcentrifuge before use; add only the supernatant to the experiment. This step will help eliminate any protein aggregates that may have formed during storage, thereby reducing nonspecific background staining. Because staining protocols vary with application, the appropriate dilution of antibody should be determined empirically. For the fluorophore-labeled antibodies a final concentration of 1-10 µg/mL should be satisfactory for most immunohistochemistry and flow cytometry applications.

    Product will be shipped at Room Temperature.

    靶标信息

    Anti-Mouse secondary antibodies are affinity-purified antibodies with well-characterized specificity for mouse immunoglobulins and are useful in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (i.e. immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents.

    仅用于科研。不用于诊断过程。未经明确授权不得转售。

     

    微信图片_20250904122753_313_89.jpg

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    图标文献和实验
    该产品被引用文献
    Invitrogen A-11029 抗体因特异性强、荧光标记性能稳定的特点,被广泛应用于细胞生物学、肿瘤学、肾病学等多个领域的研究,多篇发表在主流学术期刊的文献均使用该抗体完成实验检测。以下是部分具有代表性的引用文献,涵盖不同研究方向,具体信息如下:
     
    1. 《Fucoidan exerts protective effects against diabetic nephropathy related to spontaneous diabetes through the NF-κB signaling pathway in vivo and in vitro》
      • 发表期刊:《International Journal of Molecular Medicine》
      • 发表时间:2015 年
      • 作者:Wang Y, Nie M, Lu Y 等
      • 应用场景:研究褐藻糖胶对自发性糖尿病相关糖尿病肾病的保护作用时,借助该抗体开展免疫细胞化学染色实验,以此辅助验证 NF - κB 信号通路在发病机制及褐藻糖胶干预过程中的作用,为多糖类物质治疗糖尿病肾病提供了实验依据。
    2. 《Overlap microtubules links sister k-fibres and balance the forces on bi-oriented kinetochores》
      • 发表期刊:《Nature Communications》
      • 发表时间:2016 年
      • 作者:Kajtez J, Solomatina A, Novak M 等
      • 应用场景:在研究重叠微管如何连接姐妹动粒纤维并平衡双定向动粒上的力时,采用该抗体进行免疫细胞化学实验,以 1:100 的浓度完成相关细胞标记,助力清晰观察细胞分裂过程中微管与动粒的相互作用,为细胞分裂机制的研究提供了直观的荧光成像支持。
    3. 《Isolation and characterization of equine native MSC populations》
      • 发表期刊:《Stem Cell Research & Therapy》
      • 发表时间:2017 年
      • 作者:Esteves C, Sheldrake T, Mesquita S 等
      • 应用场景:在分离和鉴定马源天然间充质干细胞群的研究中,利用该抗体开展冰冻切片的免疫组织化学实验,用于干细胞相关标志物的荧光标记检测,为马源干细胞的特性分析及后续应用研究奠定了基础。
    4. 《Loss of ARPC1B impairs cytotoxic T lymphocyte maintenance and cytolytic activity》
      • 发表期刊:《Journal of Clinical Investigation》
      • 发表时间:2019 年
      • 作者:Randzavola L, Strege K, Juzans M 等
      • 应用场景:研究 ARPC1B 基因缺失对细胞毒性 T 淋巴细胞维持及溶细胞活性的影响时,通过该抗体完成免疫荧光染色,辅助观察 T 淋巴细胞相关蛋白的定位与表达,揭示了 ARPC1B 在免疫细胞功能调控中的关键作用。
    5. 《DAPK1 loss triggers tumor invasion in colorectal tumor cells》
      • 发表期刊:《Cell Death & Disease》
      • 发表时间:2019 年
      • 作者:Steinmann S, Kunze P, Hampel C 等
      • 应用场景:在探究 DAPK1 基因缺失引发结直肠肿瘤细胞侵袭的机制研究中,运用该抗体进行相关蛋白的荧光标记检测,为明确结直肠肿瘤侵袭的分子机制提供了可靠的实验数据支撑。
    6. 《Tspan5 enriched microdomains provide a platform for dendritic spine maturation through neuroligin - 1》
      • 发表期刊:未明确标注(文献信息节选完整)
      • 发表时间:2019 年
      • 作者:Moretto E, Longatti A, Murru L 等
      • 应用场景:研究四跨膜蛋白 5 富集的微区通过神经连接蛋白 1 促进树突棘成熟的机制时,利用该抗体的荧光标记特性完成细胞内蛋白的定位检测,助力解析神经细胞突触发育相关的分子调控网络。
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