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Apo-BRDU Flow Cytometry Detect

ion Kit; 50 assays
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  • 询价
  • APT115
  • 2026年01月11日
  • Flow Cytometry
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    • 详细信息
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    • 应用范围

      Flow Cytometry

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    • 适应物种

      All

    • 抗原来源

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    • 库存

      大量

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    • 规格

      50 assays

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    Br-dUrd Incorporation & Labeling

    Description:
    Apo-BrdU™ Flow Cytometry Detection Kit
    Trade Name:
    Chemicon (Millipore)
    Product Overview:
    The CHEMICON APO-BRDU™ Kit is a two color staining method for labeling DNA breaks and total cellular DNA to detect apoptotic cells by flow cytometry (Li et al. 1995). The kit contains the instructions and reagents required for measuring apoptosis in cells including; positive and negative control cells for assessing reagent performance; washing, reaction, and rinsing buffers for processing individual steps in the assay; terminal deoxynucleotidyl tranferase enzyme (TdT), bromodeoxyuridine triphosphate (Br-dUTP), and fluorescein labeled anti-BrdU antibody for labeling DNA breaks and Propidium Iodide/RNase A solution for counter staining the total DNA.
    Key Applications:
    Flow Cytometry
    Species Reactivity:
    All
    Usage Statement:
    Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
    Kit or Assay Type:
    Apoptosis Assays
    Components:
    • The APO-BRDU™ Kit is shipped in one container and consists of two packages. One package is shipped at ambient temperature and should be stored at 2-8°C upon arrival. The other package is styrofoam containing frozen ice packs and the reagent contents should be stored at -20°C upon arrival. Note: Upon arrival store the reagents at the appropriate temperatures.
    • Reagent bottles have color coded caps to aid in their identification. Sufficient reagents are provided to process 60 cell suspensions including 5 mL positive and 5 mL negative control cell suspensions of approximately 1 x 106 cells per mL in 70% (v/v) ethanol. The control cells are derived from a human lymphoma cell line and have been fixed as described on page 6.
    • Positive Control Cells, Brown cap
    • Negative Control Cells, White cap
    • Wash Buffer, Blue cap
    • Reaction Buffer, Green cap
    • TdT Enzyme, Yellow cap
    • Br-dUTP, Violet cap
    • Rinsing Buffer, Red cap
    • Fluorescein~PRB-1 mAb, Orange cap
    • PI/RNase Staining Buffer, Amber bottle
    Storage Conditions:
    Precautions and Warnings

    1. The components of this kit are for Research Use only and are not intended for diagnostic procedures.

    2. Positive and negative control cells contain 70% (v/v) ethanol as a preservative; wash and reaction buffer contain sodium cacodylate (dimethylarsinic) as a buffer; rinsing and PI/RNase staining buffer contain 0.05% (w/v) sodium azide as a preservative. These materials are harmful if swallowed; avoid skin contact, wash immediately with water. See Material Safety Data Sheets.

    3. TdT Enzyme will not freeze at -20oC, because it is in 50% (v/v) glycerol solution. Upon warming the TdT enzyme solution, centrifuge the tube for 30 seconds to force all the liquid to the bottom of the tube.
    Detection Methods:
    Fluorescent
    Materials Required but Not Delivered:
    1. Flow Cytometer

    2. Distilled Water

    3. 1% (w/v) paraformaldehyde (methanol free) in PBS

    4. 70% (v/v) ethanol

    5. 37°C Water Bath

    6. Ice Bucket

    7. 12 x 75 mm flow cytometry test tubes

    8. Micro-pipettor

    Product Family Information

    BrdU

    Millipore’s Anti-BrdU antibody demonstrates specificity against BrdU. See below for data, references and related products for BrdU. All Millipore antibodies are based on the expertise of Upstate & Chemicon.

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    图标文献和实验
    相关实验
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      mutations lead to abnormalities that can be detected in circulating peripheral blood cells of suspected patients by flow cytometry and the appropriate combinations of reagents and in vitro manipulations. The flow cytometry procedures that have been developed

    • A SENSITIVE METHOD FOR DETECTION OF APOPTOSIS BY SINGLE LASER FLOW CYTOMETRY

      immunofluorescence by single laser flow cytometry. J Immunol Meth 170: 145-157, 1994.   Staining for detection of apoptosis 1 x 106 PBSAz-washed cells from a single cell suspension are pelleted in a 12 X 75mm culture tube. The pellet is resuspended

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