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geneMAP™ 2019-nCoV (SARS-CoV-2) Detection Kit (nCoV-RT100)

Coronaviruses are a large family of viruses found in both animals and humans. Some infect people and are known to cause illness ranging from the common cold to more severe diseases such as Middle East Respiratory Syndrome (MERS) and Severe Acute Respiratory Syndrome (SARS).

geneMAP™ Thrombophilia Kits

The genMAP™ Thrombophilia assay offers a very simple procedure for testing the most relevant mutations implicated in the risk of an abnormality of blood coagulation, leading to increased risk for thrombosis.

geneMAP™BCR-ABL1 P210 (Mbcr) IS-MMR Detection Kit (BCR210-RT48)

Chronic myeloid leukemia (CML) is a slowly-progressing cancer characterized by the clonal myeloproliferative expansion of pluripotent hematopoietic stem cells resulting from acquisition of the fusion oncogene BCR-ABL1.

geneMAP™ FMF Kits

Familial Mediterranean Fever (FMF) is an autosomal recessive, inflammatory disorder characterized by short, recurrent attacks of fever, accompanied by pain in the abdomen, chest or joints, and erysipelas-like erythema.

geneMAP™ Leukemia Kits

The Genmark Leukemia assay offers a very simple procedure for testing the most relevant mutations implicated

geneMAP™ COVID-19 (2019-nCoV) Detection Kit V.2 (COVID19-RT100)

Coronaviruses are a large family of viruses found in both animals and humans. Some infect people and are known to cause illness ranging from the common cold to more severe diseases such as Middle East Respiratory Syndrome (MERS) and Severe Acute Respiratory Syndrome (SARS).

geneMAP™ MTB Detection Kit (MTB-RT100)

Tuberculosis (TB) remains a major public health problem worldwide. In 2015, 10.4 million new cases of TB were reported.

geneMAP™ BCR-ABL1 (p190, p210, p230) Screening Kit (BCRSCR-RT48)

BCR-ABL1 translocation can be observed in myeloproliferative neoplasms, acute leukemia of ambiguous lineage and precursor lymphoid neoplasms class as chronic myeloid leukemia (CML), acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML).

geneMAP™ HLA-B*27 Detection Kit (B27-RT50)

HLA-B molecules are cell surface proteins that play an important role in immunity. The frequency of the HLA-B27 variant is about 8% in the general Caucasian population, whereas it is found in over 90% of patients suffering from ankylosing spondylitis (AS).

geneMAP™ JAK2 V617F Mutation Detection Kit (JK14-RT50)

Somatic mutation of the JAK2 gene (JAK2 p.V617F) can be detected in a variable proportion of patients with myeloproliferative neoplasms.

geneMAP™ MTB/NTM Detection Kit (MTBN-RT100)

Tuberculosis (TB) remains a major public health problem worldwide. In 2015, 10.4 million new cases of TB were reported.

geneMAP™ HLA-B*51 Detection Kit (B51-RT50)

It was diagnosed in 1937 by Hulusi Behçet, a Turkish doctor, and is therefore referred to as Behçet’s Disease or Behçet’s Syndrome in the international literature.

geneMAP™ Celiac (DQ2, DQ8, DR4) Detection Kit (CEL-RT25)

Celiac disease is a common, familial, autoimmune gastrointestinal disease. It is caused by sensitivity to the dietary protein gluten, which is present in wheat, rye, and barley.

geneMAP™ Influenza A/B Detection Kit (INFA/B-RT50)

Influenza virus infection is a highly contagious respiratory disease that can spread easily and that is responsible for considerable morbidity and mortality each year.

geneMAP™ MPL W515A/L/K/R Mutation Detection Kit (MPL-RT25)

Myeloproliferative Leukemia Virus (MPL) appears distinctly associated with polycythemia vera (PV), essential thrombocythemia (ET) and Primary myelofibrosis (PMF).

geneMAP™ MTB/MDR Detection Kit (MTB/MDR-RT50) (Available Soon)

Drug-resistant tuberculosis is a global health problem that hinders the progress of tuberculosis eradication programs.

geneMAP™ CALR Mutation Screening Kit (CALR-RT25)

The calcium-binding endoplasmic reticulin chaperone protein, calreticulin (CALR), is somatically mutated in approximately 70% of patients with JAK2-negative essential thrombocythemia (ET) and 60% to 88% of patients with JAK2-negative primary myelofibrosis (PMF).

geneMAP™ SMN1 Exon7/8 Deletion Screening Kit (SMN1M-RT50)

Spinal muscular atrophy (SMA) is characterized by muscle weakness and atrophy resulting from progressive degeneration and loss of the anterior horn cells in the spinal cord (i.e., lower motor neurons) and the brain stem nuclei.

geneMAP™ MTB/XDR Detection Kit (MTB/XDR-RT25) (Available Soon)

Drug-resistant tuberculosis is a global health problem that hinders the progress of tuberculosis eradication programs.

geneMAP™ JAK2 Exon 12 Mutation Screening Kit (JK12-RT50)

Mutations within exon 12 of the JAK2 gene occur in most cases of JAK2 V617F-mutation negative polycythemia vera.

geneMAP™ NPM1 (mutA,B,C&D) Mutation Detection Kit (NPM-RT25)

Nucleophosmin-1 (NPM1) mutations represent the most frequent gene alteration in acute myeloid leukemia (AML).

geneMAP™ FLT3 ITD/D835Y Mutation Detection Kit (FLT3-FA25)

Mutation of the fms-like tyrosine kinase 3 gene consisting of internal tandem duplication (FLT3-ITD), which is one of the most frequent genetic alterations, occurs in 15–35% of adults with acute myeloid leukemia (AML).

geneMAP™ FLT3 D835Y Mutation Detection Kit (FLT3-RT25)

FLT3 is mutated in 11.3% of acute myeloid leukemia patients with FLT3 D835Y present in 1.28% of all acute myeloid leukemia patients.

geneMAP™ HPV Screening Kit (HPVS-RT50) (Available Soon)

Drug-resistant tuberculosis is a global health problem that hinders the progress of tuberculosis eradication programs.

geneMAP™ c-KIT D816V Mutation Detection Kit (CKT-RT25)

This test is used for qualitative detection of the KIT c.2447A>T (D816V) mutation found in most adults (>80%) with systemic mastocytosis.

geneMAP™ Borellia Detection Kit (BOR-RT50)

Lyme borreliosis is a systemic disease caused by infection with the spirochete Borrelia burgdorferi.

geneMAP™ WT1 Expression Analysis Kit (WT1-RT24)

WT1 is an important regulatory molecule involved in cell growth and development.

geneMAP™ PD-L1 Expression Analysis Kit (PDL-RT24)

So far most clinical trials have demonstrated superior efficacy of immunotherapy in advanced NSCLC, and shown a strong predictive association between PD-L1 expression levels and clinical efficacy endpoints such as overall survival, progression free survival, objective response rate.

geneMAP™ HER2 Expression Analysis Kit (HER-RT24)

The human epidermal growth factor receptor 2 gene (HER2, also known as erbB2) has been regarded a critical factor for diagnosis and effective treatment of breast cancer patients.

geneMAP™ MGMT Methylation Analysis Kit (MGM-RT50)

The MGMT Promoter Methylation Detection Kit is a methylation-specific Realtime PCR (MSP) test designed to detect and quantification O (6) -methylguanine-DNA methyltransferase (MGMT) promoter hypermethylation status in genomic DNA of glioblastoma multiform (GBM) tumors.

geneMAP™ MLH1 Methylation Analysis Kit (MLH1-RT50)

Lynch syndrome is an autosomal dominant, inherited cancer syndrome due to a germline mutation in a gene controlling DNA mismatch repair (MMR), such as MLH1, MSH2, MSH6 or PMS2.

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