Oncology services FISH assays
Oncology Services

Ultra High-resolution Pinpoint FISH Probes

KromaTiD’s Pinpoint FISH probes can also be used for ultra high-resolution FISH assays for detecting genetic abnormalities associated with cancer.By modifying hybridization conditions and eliminating daughter strand degradation. In cells that rarely divide or are non-dividing, Pinpoint FISH can be used to monitor structural rearrangements and is capable of tracking genomic loci as small as 2kbs. As opposed to BAC and many other FISH probes with limits of detection around 10kb. Pinpoint FISH probes can be used in interphase or metaphase cells with a variety of color and design options available to help you get the data you need.

Learn More About Pinpoint FISH →

{slideshow}

dGH SCREEN™ FISH probes
dGH SCREEN™

Cover Every Available Sequence with dGH SCREEN™

dGH SCREEN utilizes KromaTiD’s single stranded, synthetic probes to cover every available sequence in the genome for the ultimate unbiased assessment of potentially oncogenic rearrangements. By spanning entire chromosomes, dGH SCREEN enables researchers to directly visualize structural rearrangements anywhere in the genome, making it possible to monitor stability and other genomic hallmarks of cancer without needing to know where to look in the first place.

Used by itself or combined with dGH in-Site, SCREEN provides unbiased, whole genome data on translocations, inversions, copy number variants and other complex rearrangements in a single assay.

Learn More About dGH SCREEN →

dGH in-Site™ Targeted Assay Services
dGH in-Site™

Examine Patient Samples One Cell at a Time with
dGH in-Site™

dGH in-Site gives researchers the ability to directly visualize and characterize rearrangements at targeted loci in genetic disease patient samples. Using synthetic oligo probes and repeat-free bioinformatic design, dGH in-Site is capable of tracking translocations, inversions, copy number variants, viral integrations and other complex rearrangements with an approximate 2kb resolution.

In-site allows researchers to examine patient samples one cell at a time without having to worry about PCR biases or misrepresentative sequencing averages from heterogeneous cell populations.

Instead, as an orthogonal and complementary technique, in-Site allows you to gather the most comprehensive data available in order to help provide as many answers as possible for patients of rare or undiagnosed genetic diseases.

Learn More About dGH in-Site →

INQUIRE

INQUIRE

RESOURCES

DGH SCREEN™ DATA SHEET
DGH SCREEN™ Overview
Gene Editing Sample Report

PRODUCTS

FISH BUFFERS
PINPOINT FISH™ TP53/CEP17 KIT
SUBTELomere Pinpoint FISH™ Probes
Centromere Pinpoint FISH™ Probes
Oncology Pinpoint FISH™ Probes
HUMAN WHOLE CHROMOSOME PINPOINT FISH™ PAINT PROBES

SERVICES

DGH IN-SITE™ TARGETED ASSAY SERVICES
DGH SCREEN™ UNBIASED ASSAY SERVICES
PINPOINT FISH™ ASSAY SERVICES
Cell Culture Services
G-Banding