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Abnova/DNA (+) Control CISH Probe/1kit/CO0004

价格
面议
货号:CO0004
浏览量:127
品牌:Abnova
服务
全国联保
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商品描述
  • Specification
  • Product Description:
  • DNA (+) Control CISH Probe is designed to be used for the detection of human Alu repetitive sequences in formalin-fixed, paraffin-embedded tissue or cells by chromogenic in situ hybridization (CISH).
  • Recommend Usage:
  • Bring probe to hybridization temperature before use.
  • Supplied Product:
  • Reagent Provided:1. Digoxigenin-labeled oligonucleotides which target human Alu repetitive sequences.2. Formamide based hybridization buffer.
  • Storage Instruction:
  • Store at 2-8°C in an upright position. Return to storage conditions immediately after use.
  • Note:
  • The probe is intended to be used in combination with the CISH Implementation HRP-DAB Kit (Catalog #: KA5367), which provides necessary reagents for specimen pretreatment and post-hybridization processing.Depending on the detection system that is used, colored precipitates, which can be clearly distinguished from the background, will be observed within the cells targeted by this Probe. A positive reactivity for human Alu repetitive sequences in the target cells is indicated by a distinctly stained nucleus. Visualization of signals should be performed by light microscopy using a 10x or 20x objective. For signal evaluation, necrotic, degenerated or over-digested cells should be avoided as these cells often stain nonspecifically. In order to judge the specificity of the hybridization signals and to confirm the correct performance of the method, any hybridization should be accompanied by controls. We recommend using at least one control sample containing both true positive and negative staining cells.
  • Regulatory Status:
  • For research use only (RUO)
  • Datasheet:
  • PDF DownloadDownload
  • Applications
  • Chromogenic In Situ Hybridization (FFPE Tissue)
  • Application Image
  • Chromogenic In Situ Hybridization (FFPE Tissue)
Abnova的Abnova Diagnostics F蛋白表达系统基于小麦胚芽的真核翻译设备。小麦胚在浓缩干燥状态下储存所有翻译成分,一旦发芽就准备好进行蛋白质合成。常规的小麦胚芽提取物包含RNA N-糖苷酶三丁酸酯和其他翻译抑制剂,例如硫蛋白,核糖核酸酶,脱氧核糖核酸酶和蛋白酶。这些抑制剂来自胚乳。大量洗涤小麦胚芽以消除胚乳污染物已导致提取物具有高度的稳定性和活性。通过将具有5'cap和多(RSA)尾巴的mRNA与该提取物与专有脂质体结合使用,进行体外翻译反应产生足够量的膜蛋白,该膜蛋白被脂质体捕获,导致正确的构象和生物学功能必不可少的折叠。该系统相对于普遍使用的蛋白质表达平台(例如大肠杆菌,昆虫细胞和哺乳动物细胞)具有明显优势,这些平台都是体内系统,并且在细胞膜的约束下导致产量和稳定性低。此外,体外小麦胚芽系统适于自动化以用于高通量小分子以及生物学筛选和表征。