PHOTOPROBE® Biotin for Nucleic Acid Labeling

SKU Unit Size Price Qty
SP-1000-.5 1 kit
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PHOTOPROBE Reagents are nucleic acid labeling systems of choice for incorporating a label at multiple sites along the entire length of the nucleic acid. The nucleic acid labeling reaction does not destroy the original nucleic acid nor creates its copy. The integrity of the original sample is preserved. Single or double-stranded DNA, circular DNA, RNA, or PNA (peptide nucleic acid) can be labeled with the same reagents.

Features of PHOTOPROBE Biotin:

  • Kit labels up to 250 μg of target or up to 50 labeling reactions. 





More Information
Unit Size 1 kit
Target for Labeling DNA, PNA, RNA
Tag/Group Incorporated Biotin


Technical Information

DNA/RNA labeling is based on aryl azide chemistry in which the reagent, when exposed to heat or light, becomes activated and incorporates into the nucleic acid without base specificity. The nucleic acid labeling reaction can be carried out using a mercury vapor bulb (sun lamp), a UV lamp which produces light in the 350 nm to 370 nm range, a halogen lamp, a heating block, or a thermal cycler providing the investigator with great flexibility in experimental design.

A distinct advantage of the simple setup in each of these labeling options is the ease and economy of scaling up.

PHOTOPROBE Biotin incorporates biotin in one reaction step. PHOTOPROBE (Long Arm) Biotin has an extra long linker arm and should be used if increased distance between the sample and the tag is needed.


Kit Contents:

Each PHOTOPROBE Biotin Kit contains the following components to label up to 250 ug of nucleic acid (or to carry out up to 50 labeling reactions):

  • PHOTOPROBE Biotin Reagent
  • Tris Buffer
  • sec-Butanol
  • Biotinylated DNA Standard
  • Precipitant

Figure Legend:


CGH sum karyogram

CGH sum karyogram was created after analyzing PHOTOPROBE labeled tumor DNA from a small cell lung cancer. Biotin was detected with Vector Fluorescein Avidin D (green). Chromosomes from 15 metaphase spreads were analyzed for each hybridization. Figure provided courtesy of Dirk Korinth, Konrad Donhuijsen, Ulrike Bockmühl, and Iver Petersen, Institute of Pathology, University Hospital Charité, Berlin, Germany.


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