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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 provides ...
Result display time: 3 h
Sample volume: 4 ml
... quantitative monitoring. The Solution The Xpert NPM1 Mutation test is an automated test for quantifying the amount of mutant NPM1 mRNA transcripts (types A, B, and D in exon 12) as a ratio of NPM1 ...
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, and ...
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 PCR assay designed ...
... is a semi-automated kit for next-generation sequencing (NGS) of the exonic regions of the human genome (whole exome), covering a 37.64 Mb region, using genomic DNA extracted from whole blood and buccal swabs. The kit ...
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 disease ...
Xian Tianlong Science and Technology
... 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 single-cell ...
Sample volume: min 18.0 ml
... room temperature. It allows, from a single sample, in addition to cytopathological exams, the processing of other molecular tests for STIs. ...
... 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 -α4.2. Alpha-thalassemia ...
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 samples in vitro. The ...
... 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; namely G1691A ...
Anatolia Tani ve Biyoteknoloji Urunleri Sanayi ve Ticaret A.S.
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 than four hours. ...
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), based on the principle ...
... 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 to ISO13485 IVD ...
CyberGene AB
Result display time: 75 min
Sample volume: 0.015 ml
Single-pot duplex assay with integrated reverse transcription (RT) / cDNA synthesis and qPCR. Minimal Residual Disease determination through BCR-ABL/ABL ratio reported on the International Scale (IS) when used in conjunction with the recommended GenePath ...
... Human BRAF gene mutation detection kit (Fluorescence PCR method) Features ： - For qualitatively detect BRAF gene V600E mutation (ie 1799T>A) - Evaluate gene mutation ...
... conventional methods. This kit canbe used for the diagnosis of Y-chromosomal microdeletionsof the AZFa (sY84 and sY86), AZFb (sY127 and sY134), and AZFc (sY254 and sY255)region on azoospermic and oligozoospermic men. 32 Reactions/ Kit Applicable ...
JiangsuRepoDx Biotechnology Co., Ltd
... 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 coverage. Droplex ...
Gencurix
... “MOLgen Genetics AZF-microdeletions Kit” is an assay kit for the differentialdetermination of Y-chromosome AZF locus deletions using real-time PCR. Introduction “MOLgen Genetics ...
ADALTIS
... 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. Patients carrying ...
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. Most of the deletion ...
Result display time: 10 min - 15 min
... Hb S solubility test for screening sickle cell anaemia Pack Size 20 Tests ...
... 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 ...
Jiangsu MicroDiag Biomedicine Technology Co., Ltd.
... Product name: Pan Lung Cancer PCR Panel Format: Pre-loaded Size( test/ kit):8 Product name: Multi-Gene Mutations Detection Kit Format: Pre-loaded Size( test/ kit):6 ...
LCM Genect srl
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