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ABCA12 Break Apart探针 | ABCA12

Break Apart FISH Probe
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  • 询价
  • 辰辉创聚生物®️
  • NBPD-102170
  • 2026年05月22日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Store at 4°C for short-term, -20°C for long-term. Avoid repeated freezing and thawing cycles.

    • 保质期

      见COA

    • 英文名

      ABCA12 Break Apart FISH Probe

    • 库存

      大量

    • 供应商

      北京辰辉创聚生物技术有限公司

    • 规格

      10 Tests, 20 Tests

    产品细节图片1

    | 产品信息

    品名: NebuProbe™ ABCA12 Break Apart FISH Probe

    货号: NBPD-102170

    产品分类: 易位gene FISH Probes

    规格:10 Tests; 20 Tests; Bulk

     

    | 产品描述

    NebuProbe™ ABCA12 Break Apart FISH Probe (Cat# NBPD-102170) is designed to detect translocations, the most common genetic abnormality exhibited in cancer cells. With new gene rearrangements being continuously discovered, and their oncogenic effects elucidated, translocations have become essential cancer biomarkers.

     

    | 产品属性

    Label: Green/Red/Aqua/Orange/DIG/BIO

    Location: 2q35

    Synonym: ABCA12 Break Apart FISH Probe

    Usage: For Research Use Only.

    Storage: Store at 4°C for short-term, -20°C for long-term. Avoid repeated freezing and thawing cycles.

    ApplicationBreak apart probes are designed to detect translocations. The probes are designed to flank either side of a gene so that in the event of a translocation, the two colors will split.

     

    For Research Use Only!
    To get more information, please contact us freely.

     

    郑重声明:仅用于科学研究,不可用于诊断或治疗。
    更多产品细节,请联系我司相关客服人员。

     

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    图标文献和实验
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    • 【求助】关于ALK融合基因的检测

      walla 香港华创贸易国际有限公司北京办事处供应德国Zytolight ALK融合基因的FISH检测探针: 1、Z-2124-200 ZytoLight SPEC ALK Dual Color Break Apart Probe Green/Orange 200ul Z-2124-50 ZytoLight SPEC ALK Dual Color Break Apart Probe Green/Orange 50ul 2、Z-2117-200 ZytoLight

    • Negative Staining for Transmission Electron Microscopy

      without them breaking. This protocol is described in more detail in the section on immunolabeling. Briefly, the grids are floated onto drops of diluted antibody. washed by floating on drops of buffer, and then floated on drops of diluted visualization probe. We normally

    • 小RNA的Northern BLOT

      with syringe. Un-clamp gel.  Pry apart glass plates with spatula. Cut off upper right corner of gel. Place saran wrap on top of gel, flip over and remove other glass plate. (Be sure to wet the gel with a little TBE so it does not dry out and break

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