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... amplification reagents intended for the nucleic acid multiplex amplification of 40 regions of the CFTR gene (regions for some mutations are combined) in only one reaction. The INNO-LiPA CFTR iage approach ...
OncoCompassTM Target Cancer Mutation Profiling Liquid Kit (24 Test/kit) OncoCompassTM Target Cancer Mutation Profiling Liquid Kit ...
OncoScreenTM Plus Cancer Mutation Profiling Tissue Kit (48 test kits/box) This kit is intended to be used for the qualitative detection of multiple ...
Result display time: 8 min - 9 min
Sample volume: 2 ml - 5 ml
Specificity: 70 % - 74 %
... peripheral EDTA anticoagulant blood as the test specimen to detect the copy number of SMN1 at the 7th exon and (or) the 8th exon in human genomic DNA. Spinal muscular atrophy (SMA) is an autosomal recessive genetic ...
Result display time: 60 min - 90 min
This kit is suitable for the qualitative detection of Mycobacterium tuberculosis DNA in human sputum samples in vitro, as well as the homozygous mutation in the 507-533 amino acid codon region of the ...
Jiangsu Macro micro-test Medical Technology
Result display time: 60 min - 90 min
Specificity: 97 % - 99 %
Sensitivity: 97 % - 99 %
This kit is used to in vitro qualitative detection of 14 types of ROS1 fusion gene mutations in human non-small cell lung cancer samples (Table 1). The test results are for clinical reference ...
Jiangsu Macro micro-test Medical Technology
Result display time: 60 min - 90 min
Specificity: 97 % - 99 %
Sensitivity: 97 % - 99 %
This kit is intended for in vitro qualitative detection of 8 mutations in codons 12 and 13 of K-ras gene in extracted DNA from human paraffin-embedded pathological sections. Point mutations ...
Jiangsu Macro micro-test Medical Technology
... and SuperSTaR QF-PCR kits ChromoQuant QF-PCR tests for prenatal diagnostics Detection of aneuploidy in chromosomes 13, 18, 21, X and Y ChromoQuant® is CE marked for IVD use and produced according ...
... ThermoFisher Scientific Product Numbers: ChromoQuant Optima PLUS: 531.001-26, 26 tests ChromoQuant Optima STaR PLUS: 514.531-26, 26 tests of Optima PLUS and 26 tests of STaR Optima 1
... solution to identify gene mutation in different types of cancer to facilitate targeted therapy. By incorporating Droplet Digital PCR technology, Droplex shows improved sensitivity with wider mutation ...
Gencurix
... treatment that is tailored for individual patients. Regulatory status - IVD-CDx Mutation variants - 28 Storage Temp - -20°C (+/- 3°C) 4 well-reactions/test (24 tests/kit)
Gencurix
... tailored for individual patients. Regulatory status - IVD Compatible Mutation variants - 6 Storage Temp - -20°C (+/-3°C) 3 well-reactions/test (32 tests/kit)
Gencurix
1. The deletion of 20q was found in MPD, MDS(4%), AML(1%) and other diseases. It has a good prognosis. 2. The deletion of 12 microregions of 20q was found in MPD and MDS.
Celnovte Biotechnology Co., Ltd.
1. The deletion of the entire chromosome 7 or the entire long arm 7q is a recurrent abnormality of MDS. It happens in approximately 5-10% AML(M4 and M6) ,in approximately 15% adult MDS, 40% child MDS and 50% treatment-related AML/MDS. ...
Celnovte Biotechnology Co., Ltd.
1.5Q long arm deletion is the most common abnormal in AML and MDS. The Abnormalities on chromosome No. 5 is accounted for more than up to 40% of treatment-related MDS. 2.The internal deletion of 5Q (5Q31-Q33) occurs in 10-15% of MDS ...
Celnovte Biotechnology Co., Ltd.
Kit for detection and genotyping of the G20120A mutation in the human gene coding for Coagulation Factor II by Real-Time PCR The kit includes: Ready-to-use reagents ...
AB Analitica
Kit for detection and genotyping of the G1691A mutation (Leiden) in the human gene coding for Coagulation Factor V by Real-Time PCR The kit includes: Ready-to-use reagents ...
AB Analitica
Kit for detection and genotyping of the C282Y mutation in the HFE gene by Real-Time PCR The kit includes: Ready-to-use reagents for Real-Time PCR Positive controls ...
AB Analitica
... tuberculosis and 25 mutations associated with MDR-TB Wild-type Control WTC[1](Wild-type Control) and Internal Control (IC) for assay validity DNA extraction solution Reagent for DNA Detection ...
... enrichment technologies Why Choose Instant NanoBiosensors Custom Multiplex NGS Panels? Service cost (from design to kits) - Low Per Kits price - Low (ISO certification factory) Input Sample ...
... for the presence of EGFR mutations prior to TKI treatment. Patients carrying EGFR mutations known as `activating mutations´ may benefit from first- or second- or third-generation TKIs. ...
... acid substitution mutations on exon 21; exon 18-point mutations (G719S or G719C) account for about 5%; Insertion mutations on exon 20 accounted for about 1% of the total. And some mutations ...
... acid substitution mutations on exon 21; exon 18-point mutations (G719S or G719C) account for about 5%. Insertion mutations on exon 20 accounted for about 1% of the total. And some mutations ...
Result display time: 2 min
Specificity: 100 %
Sensitivity: 98.5, 100 %
... with higher risk of thrombosis and embolisms. Variant detection by genetic testing is important in patients with hypercoagulability to provide adapted therapy. Coagulation ELITe MGB® Kit is a real-time ...
Sensitivity: 95 %
... Plasma-SeqSensei™ IVD Software. The kit covers key gene mutations such as AKT1, ERBB2, ESR1, KRAS, PIK3CA, and TP53 to detect established and emerging predictive markers, resistance mutations, ...
Result display time: 60 min
... additional variants, such as SMN1 gene duplication events and disease modifier in SMN2. The AmplideX® PCR/CE SMN1/2 Plus Kit* revolutionizes the analysis of these two genes by delivering comprehensive results in less ...
Asuragen
Result display time: 60, 30, 5 min
Sample volume: 0.025 ml
... deficiency as well. Measurement of 17-Alpha-OHP is therefore valuable in the initial diagnosis of CAH. The DRG 17-OH Progesterone ELISA Kit is a solid phase enzyme-linked immunosorbent assay (ELISA), ...
... sensitive and customizable panels that enable true multi-omics analysis on the Tapestri Platform. Whether identifying co-mutation patterns and zygosity in subclones or cellular identities and subtle cell states, Tapestri ...
The kit is used for in vitro qualitative detection of whether whole blood DNA samples carry α-thalassaemia deletion genes. The kit can detect three α-thalassemia deleted gene including --SEA, -α3.7and ...
Yaneng Bioscience (Shenzhen) Co., Ltd.
... Leukocyte Antigen B27 Nucleic Acid Test Kit Predicator of Ankylosing Spondylitis This product is used for the qualitative detection of HLA-B27 subtype B27*04 and B27*05 subtype in human whole blood ...
Thrombophilia is a multi-factor disease revealing several predisposing genetic and environmental risk factors. Protein C deficiency and Protein S deficiency belong to the congenital thrombophilic risk factors. AESKU.DIAGNOSTICS ...
... Panel Kit v1 detects Factor II mutation in the 3’UTR region of FII gene; namely G20210A (prothrombin mutation /a change of guanine to adenine) and Factor V Leiden mutations; ...
Anatolia Tani ve Biyoteknoloji Urunleri Sanayi ve Ticaret A.S.
Test detects 22 human beta globin mutations in blood or oral buccal samples. The kit identifies the most relevant mutations in the beta globin genes in the Southeast Asia region.
Chromosome 6q amplifications encompassing 6q21-22 have been observed in MM including the same region as in CLL. Amplification including band 15q22 has been reported in MM. The 15q22 specific FISH probe is optimized to detect copy numbers ...
Result display time: 90 min
... Descripption Adopting the ARMS-PCR method, this kit completely covers 45 drug susceptibility and resistance mutations in EGFR exons 18-21, and is presently one of the EGFR gene mutation ...
Human BRAF gene mutation detection kit (Fluorescence PCR method) Features ： - For qualitatively detect BRAF gene V600E mutation (ie 1799T>A) - Evaluate gene mutation ...
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