New launch! | Five high performance IVT Kits, covering the full spectrum of functionalized mRNA synthesis | Code baseScribe30 for 30% off

New launch! | Five high performance IVT Kits, covering the full spectrum of functionalized mRNA synthesis | Code baseScribe30 for 30% off

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DNA FISH Kit

Preparation of fluorescent-labeled DNA probes by PCR

Size Catalog No. Price
Dye 488 BCK-DNA-FISH-488  500,00
Dye 555 BCK-DNA-FISH-555  500,00
Dye 594 BCK-DNA-FISH-594  500,00
Dye 647 BCK-DNA-FISH-647  500,00
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Chemical Properties

  • Shelf Life

    12 months unopened after receipt

  • Storage Conditions

    – 20 °C

  • Physical State

    kit system made of different components

  • CAS Number

    n.a.

  • Excitation (max)

    Dye 488: 496 nm | Dye 555: 546 nm | Dye 594: 584 nm | Dye 647: 643 nm

  • Emission (max)

    Dye 488: 516 nm | Dye 555: 579 nm | Dye 594: 603 nm | Dye 647: 662 nm

  • Ɛ (max)

    Dye 488: 83.000 cm-1M-1 | Dye 555: 91.000 cm-1M-1 | Dye 594: 110.000 cm-1M-1 | Dye 647: 250.000 cm-1M-1

  • Preparation/Handling

    please see user manual of the kit

Product Information

HighEfficiency Fluorescent DNA Probe Generation

The ClickTech DNA FISH Kit enables fast, reliable, and highly efficient preparation of fluorescently labeled DNA probes for Fluorescence in situ Hybridization (FISH) applications. FISH is an essential cytogenetic method for detecting and localizing specific DNA or RNA sequences in cells or tissues, widely used in basic research as well as in clinical contexts such as cancer diagnostics, genetic syndrome analysis, and prenatal screening.

Traditional FISH methods often struggle with weak fluorescence due to low incorporation of dye‑labeled nucleotides. In contrast, baseclick’s technology incorporates alkyne‑modified EdUTP directly during PCR, allowing dense downstream dye conjugation through click chemistry. This results in remarkably bright, saturated probes, producing strong, clean signals even in challenging chromatin environments.
fluorescence in situ hybridization

How the ClickTech DNA FISH Kit Works

During PCR amplification, the provided Ethynyl Polymerase incorporates a mixture of natural dNTPs and alkyne‑modified EdUTP, generating a “clickable” DNA amplicon. In a subsequent step, the included click reagents covalently attach the fluorescent azide dye of your choice (488, 555, 594, or 647) resulting in intense, stable, and uniformly labeled DNA FISH probes.

principle of the DNA FISH Kits

  • High labeling density: Produces bright, sensitive probes with significantly improved signal‑to‑noise ratio.
  • Universal dye options: Four clickable dyes included—green (488), yellow (555), orange (594), red (647)—allowing flexible multicolor FISH assay design.
  • The complete workflow in one kit: Contains all reagents for PCR, click labeling, and probe generation.
  • Efficient performance: Supports 20 PCR reactions (50 µL each) and 40 labeling reactions for independent FISH experiments.
  • High-quality fluorescence characteristics:
    • 488: Ex 496 nm / Em 516 nm
    • 555: Ex 546 nm / Em 579 nm
    • 594: Ex 584 nm / Em 603 nm
    • 647: Ex 643 nm / Em 662 nm
  • Storage-friendly: Long shelf life of 12 months when stored at –20 °C.

Applications

  1. Cancer Cytogenetics & Oncology Research

FISH is widely used in diagnosing and characterizing cancer, including:

    • Detection of translocations (e.g., BCR‑ABL)
    • Copy number variations (CNVs)
    • Gene amplification (e.g., HER2)

The high sensitivity of ClickTech probes enhances the detection of subtle aberrations in heterogeneous tumor samples.

  1. Genetic Syndrome Diagnostics

FISH remains indispensable for identifying chromosomal abnormalities that cause genetic syndromes. Applications include detection of:

    • Microdeletions
    • Trisomies
    • Structural rearrangements

The ClickTech kit’s high labeling density ensures reliable detection even in prenatal cytogenetic samples.

  1. Prenatal & Postnatal Screening

ClickTech DNA FISH probes are ideal for rapid screening assays in:

    • Amniocytes
    • Chorionic villi
    • Neonatal blood smear nuclei

The strong signal allows accurate detection even on low‑quality or partially condensed samples.

  1. SingleCell Genomics & Nuclear Architecture Mapping

Researchers studying 3D genome organization or nuclear compartmentalization can benefit from the kit’s:

    • High probe intensity
    • Reliable locus targeting

This enables elegant visualization of chromosomal territories and long‑range interactions in single nuclei.

  1. Detection of Viral Integration or Transgenic Insertions

Bright DNA FISH probes allow precise identification of exogenous sequences in:

    • Viral integration studies
    • CRISPR/Cas9 genome engineering validation
    • Stable transfection screening workflows
  1. Chromosomal Spread Analyses in Basic Research

For routine cytogenetic studies involving metaphase spreads, the ClickTech DNA FISH Kit delivers superior clarity, ideal for:

    • Karyotyping research
    • Evolutionary biology
    • Comparative genomics
  1. Diagnostic and Research Lab Multiplex Panels

Because the dyes span the green‑to‑far‑red range, the kit supports robust multiplex FISH applications such as:

    • 4‑locus panels
    • Fusion gene co‑localization
    • Multi‑color chromosome painting

 

LITERATURE

Orthogonal End Labelling of Oligonucleotides through Dual Incorporation of Click-Reactive NTP Analogues. E. Schönegger et al., 2024, ChemBioChem., Vol. 25(1), e202300701.

https://doi.org/10.1002/cbic.202300701

Divergent Synthesis of Ultrabright and Dendritic Xanthenes for Enhanced Click-Chemistry-Based Bioimaging. L. Montiel et al., 2023, Eur. J., Vol. 29(5), e202202633.

https://doi.org/10.1002/chem.202202633

Click Chemistry Enables Rapid Amplification of Full-Length Reverse Transcripts for Long-Read Third Generation Sequencing. E. Schönegger et al., 2022, Bioconjugate Chem., 33(10), p. 1789–1795.

https://doi.org/10.1021/acs.bioconjchem.2c00353

ClampFISH detects individual nucleic acid molecules using click chemistry–based amplification. S. H. Rouhanifard et al., 2019, Biotechnol., Vol 37, p. 84–89.

https://doi.org/10.1038/nbt.4286

FAQ

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