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Epigenetics and Nuclear Signaling DNA / RNA DNA / Nucleotides

DRAQ7™ (ab109202)

Price and availability

184 272 ₸

Availability

Order now and get it on Wednesday February 24, 2021

DRAQ7™ (ab109202)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

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Overview

  • Product name

    DRAQ7™
  • Description

    DRAQ7™
  • Tested applications

    Suitable for: FM, Flow Cyt, ICC/IFmore details
  • General notes

    DRAQ7™ is a far-red fluorescent dye that only stains the nuclei in dead and permeabilized cells and can be used in combination with common labels such as GFP or FITC.

    DRAQ7 is the ideal tool to study dead or membrane-compromised cells because it does not enter intact, live cells. It is an ideal replacement for propidium iodide and 7-AAD, as is not excited by UV light and has no emission overlap with PE / PE homologues.

    Key features of DRAQ7 include:

    • Rapid staining of dsDNA/ nuclei of dead or permeabilized cells
    • Low photobleaching
    • It can be used in most cell types, eukaryotic and prokaryotic: mammalian, bacterial, parasitic, plant, etc ...
    • Non-toxic in long-term culture
    • Can be combined with "live" dyes
    • No compensation needed with common FITC/GFP + PE combinations in flow cytometry
    • No wash or RNase treatment needed.

    SPECTRAL PROPERTIES

    Excitation:

    • 633 and 647 nm line optimal (Exmax 599 / 644 nm)
    • 488, 514 and 568 nm lines, sub-optimal (only by flow cytometry)

    Emission (instrument dependent):

    • 665 nm to infra-red max 678 nm / 697 nm intercalated with dsDNA)
    • Minimal overlap with vis range e.g. GFP and FITC
    • Em. filters may include 695L, 715LP or 780 LP

    Multi-wavelength imaging with UV / vis fluorochromes

    • No fluorescence enhancement upon DNA binding
    • Low photo-bleaching effect
    • Compatible with optics of flow, laser scanning cytometers and confocal and lamp-based fluoroscence microscopes

Properties

  • Form

    Liquid
  • Storage instructions

    Store at +4°C. Do Not Freeze. Store In the Dark.
  • Concentration information loading...
  • Research areas

    • Epigenetics and Nuclear Signaling
    • DNA / RNA
    • DNA / Nucleotides
    • Kits/ Lysates/ Other
    • Tools and Reagents
    • IHC Tools/ Reagents
    • Kits/ Lysates/ Other
    • Tools and Reagents
    • Fluorescent dyes and reagents
    • Kits/ Lysates/ Other
    • Kits
    • Cell Staining Kits
    • Fluorescent
    • Kits/ Lysates/ Other
    • Kits
    • Cell Staining Kits
    • Nuclear

Images

  • Flow Cytometry - DRAQ7™ (ab109202)
    Flow Cytometry - DRAQ7™ (ab109202)
    Jurkat cells exposed to 1µM staurosporine for 24 hours show DRAQ7™ staining (top half of the plot). These cells have compromised membranes that allow entry of DRAQ7™ in the cells.
  • Immunohistochemistry (Frozen sections) - DRAQ7™ (ab109202)
    Immunohistochemistry (Frozen sections) - DRAQ7™ (ab109202) Courtesy of Dr. Shaohua Li, UMDNJ-Robert Wood Johnson Medical School

    Sample: mouse embryonic stem cell-differentiated embryoid bodies (EBs)
    Preparation:

    • Fix in 3%PFA in PBS for 30 min at RT
    • Incubate in 7.5% sucrose-PBS for 3h at RT
    • Incubate in 15% sucrose-PBS at 4 degree Celsius overnight
    • Embed the EBs in tissue-Tek OCT compound
    • Cut frozen sections to 4-20 μm thickness

    Primary antibody: Rabbit anti-laminin alpha 1, 1:400
    Secondary antibody: Goat anti-rabbit IgG - H&L (AMCA) (ab123435)

    Nuclei were counterstained stained with DRAQ7™ (ab109202)

  • Immunohistochemistry (Frozen sections) - DRAQ7™ (ab109202)
    Immunohistochemistry (Frozen sections) - DRAQ7™ (ab109202) Courtesy of Dr. Shaohua Li, UMDNJ-Robert Wood Johnson Medical School

    Sample: mouse embryonic stem cell-differentiated embryoid bodies (EBs)

    Preparation:

    • Fix in 3%PFA in PBS for 30 min at RT
    • Incubate in 7.5% sucrose-PBS for 3h at RT
    • Incubate in 15% sucrose-PBS at 4 degree Celsius overnight
    • Embed the EBs in tissue-Tek OCT compound
    • Cut frozen sections to 4-20 μm thickness


    Primary antibody: Rabbit anti-laminin alpha 1, 1:400
    Secondary antibody: Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (FITC) (ab97050), 1:200
    F-actin was stained with
    CytoPainter F-actin staining kit (blue) (ab112124), 1:1000
    Nuclei were counterstained stained with DRAQ7TM, 1:1000

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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