Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More

BD Biosciences™ DAPI Solution (RUO)

Catalog No. BDB564907
Click to view available options
Quantity:
1 mg

Nucleic acid stain that binds to A-T rich regions of DNA along the minor groove.

  • Nucleic acid stain that binds to A-T rich regions of DNA along the minor groove.
  • DAPI is predominantly impermeant to live cells, allowing it to be used as a viability dye in unfixed cells to discriminate intact from membrane-compromised cells.
  • Note, however, that high concentrations of the dye may still enter intact cells.
  • Additionally, DAPI may be used to analyze DNA content in fixed cells, or as a nuclear counterstain in imaging or flow cytometry.
  • When bound to double-stranded DNA, DAPI has an excitation wavelength maximum of 358 nm and an emission maximum of 461 nm.
  • DAPI is also well excited by the violet laser line (eg, 405 nm). Note that DAPI also binds RNA.
  • Under these conditions, DAPI emits maximally at 500 nm, but with less intensity than when bound to double-stranded DNA.
TRUSTED_SUSTAINABILITY

Specifications

Concentration 1.0 mg/mL
Stain Type Nucleic acid stain
For Use With (Application) Flow cytometry, bioimaging, immunofluorescence
Quantity 1 mg
Storage Requirements Avoid multiple freeze-thaws of product. The product should be kept undiluted at -20°C for long term storage, and it may be kept undiluted at 4°C for short term storage.
WARNING: Reproductive Harm - www.P65Warnings.ca.gov
Product Content Correction

Your input is important to us. Please complete this form to provide feedback related to the content on this product.

Product Title

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.

Your feedback has been submitted: Thank you for helping us improve our website.