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Probe Panel
ALL Adult
Adult acute lymphoblastic leukemia includes genetically diverse subtypes, with probe panels supporting investigation of recurrent alterations tied to risk and disease behavior.
Clinical Probe Collections
Disease Probes
Discover expertly designed FISH probes tailored to specific disease areas, making it easier to move from question to assay with confidence. From leukemias and lymphomas to solid tumor applications, this library is built to help your team find the right starting point quickly.
Showing 19 disease areas
02
Probe Panel
ALL Pediatric
Acute lymphoblastic leukemia accounts for most childhood leukemia diagnoses, with outcomes and risk groups shaped heavily by distinct underlying chromosomal lesions.
03
Probe Panel
ALL Ph-like
BCR-ABL1 fusion defines a high-risk subset of adult acute lymphoblastic leukemia and remains a major focus for disease classification and targeted investigation.
04
Probe Panel
AML Standard
Acute myeloid leukemia panels help profile recurrent chromosome changes and structural abnormalities that shape diagnosis, classification, and downstream testing workflows.
05
Probe Panel
Barrett's Esophagus
Barrett’s esophagus can progress to esophageal adenocarcinoma, and FISH helps reveal genomic instability and early high-risk changes tied to that transition.
06
Probe Panel
Bladder
Bladder cancer research often focuses on copy number gains, losses, and locus-specific abnormalities that can help distinguish disease-associated genomic patterns.
07
Probe Panel
Breast
Breast cancer probe collections support evaluation of clinically relevant amplifications and structural events involved in tumor biology and disease stratification.
08
Probe Panel
CLL Probes
Chronic lymphocytic leukemia is the most common adult leukemia, with recurrent deletions involving 11q, 13q, and 17p, plus trisomy 12 in a meaningful subset of cases.
09
Probe Panel
Eosinophilia
Eosinophilia-associated panels help investigate rearrangements and chromosomal events linked to myeloid and lymphoid neoplasms with eosinophilic involvement.
10
Probe Panel
Glioblastoma
Glioblastoma studies frequently examine hallmark gains, losses, and oncogene-associated changes that contribute to aggressive tumor progression in the central nervous system.
11
Probe Panel
Lung
Lung cancer probe panels support investigation of recurrent amplifications, deletions, and other genomic changes relevant to tumor classification and translational research.
12
Probe Panel
MDS
Myelodysplastic syndrome panels help assess recurrent chromosome losses, gains, and structural abnormalities associated with clonal hematopoietic disease.
13
Probe Panel
Melanoma
Melanoma-focused probes support evaluation of genomic instability and copy number changes that can help distinguish malignant progression in melanocytic lesions.
14
Probe Panel
Multiple Myeloma
Multiple myeloma is driven by a complex landscape of copy number changes, IGH translocations, and tumor suppressor losses that influence progression and treatment response.
15
Probe Panel
Multiple Myeloma Reflex
IGH rearrangements are early disease-initiating events in multiple myeloma and MGUS, with recurrent partners including MAF, MAFB, CCND1, and FGFR3.
16
Probe Panel
NHL
Non-Hodgkin lymphoma panels help study recurrent rearrangements and copy number changes across genetically distinct lymphoma subtypes.
17
Probe Panel
Ovarian
Ovarian cancer collections support investigation of genomic gains, losses, and locus-specific abnormalities involved in tumor development and progression.
18
Probe Panel
Prenatal
Prenatal probe panels support targeted chromosome analysis for common aneuploidies and other abnormalities relevant to rapid prenatal assessment workflows.
19
Probe Panel
T-ALL
T-cell acute lymphoblastic leukemia panels help investigate recurrent chromosomal changes and gene-associated abnormalities involved in leukemic transformation.
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