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ReadiUse™预活化PE-iFluor?660串联染料
物品单位 价格 品牌
4368 AAT Bioquest
  • 产地:American
  • 型号:1 mg
  • 货号:CS2579
  • 发布日期: 2022-03-01
  • 更新日期: 2022-03-28
产品详细说明
产地 American
品牌 AAT Bioquest
货号 CS2579
用途范围 Research Grade
纯度 98%%
CAS编号
规格 1 mg
是否进口
简要概述

R-藻红蛋白(PE)是从红藻中分离出来的。它的主要吸收峰在565 nm,次要峰在496和545 nm。我们的PE-iFluor™660串联染料是一种出色的新颜色,由于其独特的光谱特性而已被验证用于光谱流式细胞仪应用。ReadiUse™预活化的PE-iFluor™660 串联染料是一种活化的PE蛋白,与常规PE相比,可以很容易地偶联到抗体上,具有更高的结合产率。它为制备PE-iFluor™660串联标记的抗体结合物提供了方便的工具,该结合物可用光谱流式细胞仪检测。



产品说明书

染色样本分析

操作步骤

使用Buccutite™MTA制备预活化的抗体
  1. 在DMSO中以约10 mg / mL的浓度重建Buccutite™MTA。
    注意:将未使用的MTA存放在-20°C;它最多可用于两个冷冻和解冻循环。
  2. 在pH = 8.5-9.0缓冲液中以1 mg / ml以上的浓度制备目标抗体(Ab)。
  3. 将MTA以8-10 μg MTA / 100 μg Ab的比例添加到Ab溶液中。
  4. 充分混合并在室温下反应60分钟,在反应过程中旋转。
  5. 用脱盐柱纯化反应混合物,以除去任何未反应的MTA。将缓冲液更换为PBS或您选择的其他缓冲液。
  6. 收集MTA活化的抗体。通过原始起始量的70%产率估算浓度。 

 

与预活化的PE-iFluor™660串联在一起
  1. 将预活化的PE-iFluor™660串联溶液以100 μL ddH2O的浓度重新配制至10 mg / mL。
    注意:重建的预活化PE-iFluor™660 Tandem不稳定,不能保存超过一个月。
  2. 以300μg PE-iFluor™660 Tandem / 100 μg MTA活化的Ab的比例直接将预激活的PE-iFluor™660 串联染料添加到MTA活化的目标Ab溶液中。
  3. 在室温下将混合物旋转1-2小时。
  4. Ab / PE--iFluor™660串联缀合物现已准备就绪。
    注意:抗体结合物应在载体蛋白(例如0.1%牛血清白蛋白)和0.02-0.05%叠氮化钠存在的情况下以> 0.5 mg / mL的浓度保存。
    注意:Ab / PE-iFluor™660串联可在4°C下保存两个月。
  5. 可选:Ab / PE-iFluor™660串联可通过尺寸排阻色谱法进一步纯化以获得更好的性能。 

 

图示

图1.我们预活化的PE-iFluor™660串联染料已通过我们的Buccutite™FOL(提供)进行了预改性。您的抗体(或其他蛋白质)已通过我们的Buccutite™MTA(作为免费样品提供)进行了修饰,以提供经MTA修饰的蛋白质(例如抗体)。MTA修饰的蛋白质易于与FOL修饰的PE-iFluor™660串联抗体(提供)反应,以比SMCC化学方法高得多的产率得到所需的PE-iFluor™660串联抗体结合物。此外,我们的预活化PE-iFluor™660串联反应与MTA改性的生物聚合物反应的浓度远低于SMCC化学反应。

 

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Analysis of Phospholipids, Lysophospholipids, and Their Linked Fatty Acyl Chains in Yellow Lupin Seeds (Lupinus luteus L.) by Liquid Chromatography and Tandem Mass Spectrometry.
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One-Pot Fabrication of Pd Nanoparticles@Covalent-Organic-Framework-Derived Hollow Polyamine Spheres as a Synergistic Catalyst for Tandem Catalysis.
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Supercritical CO2 Extraction and Identification of Ginsenosides in Russian and North Korean Ginseng by HPLC with Tandem Mass Spectrometry.
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Analysis of oxidised and glycated aminophospholipids: Complete structural characterisation by C30 liquid chromatography-high resolution tandem mass spectrometry.
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Fast and Quantitative Phospholipidomic Analysis of SH-SY5Y Neuroblastoma Cell Cultures Using Liquid Chromatography-Tandem Mass Spectrometry and 31P Nuclear Magnetic Resonance.
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