Web Analytics
Products - Diagnostic Testing Solutions for Hematologic Malignancies - Invivoscribe
Products – Diagnostic Testing Solutions for Hematologic Malignancies2026-10-20T16:03:25-07:00
PRODUCTS

Diagnostic Testing Solutions for Hematologic Malignancies

PRODUCTS

Diagnostic Testing Solutions for Hematologic Malignancies

Precision Oncology Diagnostics

Invivoscribe provides globally standardized hemato-oncology assay kits and workflow solutions for hematologic malignancy diagnostic testing in clinical laboratories and researchers in the areas of leukemia, lymphoma, and myeloma.

Our cGMP portfolio includes IVDR and RUO molecular diagnostics products. We offer kits for sample preparation, companion diagnostics, clonality testing, and MRD testing solutions, reagents, controls, and bioinformatics software tools designed to support precision oncology programs from assay implementation through reporting.

Precision Oncology Diagnostics

Invivoscribe provides globally standardized hemato-oncology assay kits and workflow solutions for hematologic malignancy diagnostic testing in clinical laboratories and researchers in the areas of leukemia, lymphoma, and myeloma.
Our cGMP portfolio includes IVDR and RUO molecular diagnostics products. We offer kits for sample preparation, companion diagnostics, clonality testing and MRD testing solutions, reagents, controls, and bioinformatics software tools designed to support precision oncology programs from assay implementation through reporting.

Next-Generation Sequencing

Next-Generation Sequencing

Next-generation sequencing (NGS) is revolutionizing precision medicine, enabling objective identification and tracking of genetic alterations in longitudinal studies. NGS testing for hematologic malignancies strengthens diagnosis, prognosis, risk stratification, and disease monitoring. When used for ultra-sensitive measurable residual disease (MRD) assessment, NGS can align treatment strategies with molecular drivers of disease and inform critical therapy decisions, such as bone marrow transplant operations.

Next-generation sequencing (NGS) is revolutionizing precision medicine, enabling objective identification and tracking of genetic alterations in longitudinal studies. NGS testing for hematologic malignancies strengthens diagnosis, prognosis, risk stratification, and disease monitoring. When used for ultra-sensitive measurable residual disease (MRD) assessment, NGS can align treatment strategies with molecular drivers of disease and inform critical therapy decisions, such as bone marrow transplant operations.

ABI Fluorescence Detection

ABI Fluorescence Detection

We offer a comprehensive portfolio of PCR-based kits for hematologic malignancy diagnostic testing, including B- and T-cell clonality, mutation, and translocation assays that support accurate assessment of lymphoproliferative and myeloproliferative neoplasm disorders.

Many of our assays feature advanced primer designs developed by the EuroClonality/BIOMED-2 group and validated through large multicenter studies, delivering proven reliability, reproducibility, and high-confidence detection across gene rearrangements and mutations.

We offer a comprehensive portfolio of PCR-based kits for hematologic malignancy diagnostic testing, including B- and T-cell clonality, mutation, and translocation assays that support accurate assessment of lymphoproliferative and myeloproliferative neoplasm disorders.

Many of our assays feature advanced primer designs developed by the EuroClonality/BIOMED-2 group and validated through large multicenter studies, delivering proven reliability, reproducibility, and high-confidence detection across gene rearrangements and mutations.

Clonality

FLT3

Translocations

Gel Detection

Gel Detection

We exclusively offer a comprehensive selection of PCR-based RUO leukemia, myeloma and lymphoma assay kits for gel detection, including targeted FLT3 ITD and TKD mutation assays, B- and T-cell clonality assays (based on EuroClonality/BIOMED-2 Concerted Action BMH4-CT98-3936), and translocation assays.

We exclusively offer a comprehensive selection of PCR-based RUO leukemia, myeloma and lymphoma assay kits for gel detection, including targeted FLT3 ITD and TKD mutation assays, B- and T-cell clonality assays (based on EuroClonality/BIOMED-2 Concerted Action BMH4-CT98-3936), and translocation assays.

Controls & Reagents

Controls & Reagents

lnvivoscribe offers an extensive range of Assay Specific Reagents (ASRs), General Purpose Reagents (GPRs), enzymes and Research Use Only (RUO) nucleic acid controls – the assays and reagents foundation for reliable hematologic malignancy diagnostic testing workflows.

lnvivoscribe offers an extensive range of Assay Specific Reagents (ASRs), General Purpose Reagents (GPRs), enzymes and Research Use Only (RUO) nucleic acid controls – the assays and reagents foundation for reliable hematologic malignancy diagnostic testing workflows.

Companion Diagnostics (CDx)

Companion Diagnostics (CDx)

The LeukoStrat® CDx FLT3 Mutation Assay is a globally standardized in vitro diagnostic (IVDR) PCR-based product designed to identify AML patients with mutations in the FLT3 gene who may benefit from targeted treatment.

Enhance Your Blood Cancer Diagnostic Testing

Reach out to Invivoscribe today to learn how our standardized products can support your lab’s hematologic malignancy diagnostic testing objectives. Our experts will help you select the optimal assay and workflow for your research or clinical needs.

Enhance Your Blood Cancer Diagnostic Testing

Reach out to Invivoscribe today to learn how our standardized products can support your lab’s hematologic malignancy diagnostic testing objectives. Our experts will help you select the optimal assay and workflow for your research or clinical needs.
PRODUCTS

Related Articles

PRODUCTS

Related Articles

FAQs

Illumina’s MiSeq™, MiSeq™ i100, and NextSeq™ instruments have been proven to work with our assay kits. These same assay kits have been successfully run on Complete Genomics G99 and Element’s AVITI systems with minor modifications.

Invivoscribe has validated the ABI 310, 3100 and 3500 instrument series for many of our capillary electrophoresis detection assays. Many of our capillary electrophoresis assays are also compatible with Thermo Fisher’s SeqStudioTM Flex platform.

Our standardized products, including the CE-marked IVDR test kits, controls, and software, are designed for high reproducibility in hemato-oncology testing. They support streamlined workflows, reduce inter-laboratory variability, and generate objective hematologic malignancy diagnostic testing results across decentralized testing laboratories.

These assays enable the PCR-based assessment of FLT3 ITD/TKD mutations, translocations, and clonality markers, supporting molecular oncology testing for leukemia, lymphoma, and myeloma. They support exploratory research on chromosomal abnormalities, with ISO 13485 controls and a framework for subsequent clinical validation.