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The cma practice test of CapitalBio Technology uses Affymetrix GeneChip System 3000Dx and CytoScan 750K chip, it can not only provide accurate detection of chromosomal gene abnormalities, and provide an effective diagnostic basis for clinical birth defects, but also provide corresponding value-added services of prenatal data analysis and report interpretation, which is more convenient for clinicians' daily diagnosis and practical application. Features of CMA Detection ThermoFisher Affymetrix GeneChip System 3000Dx (GCS 3000Dx) chip system provides accurate and rapid birth defect diagnosis services. It is the most reliable platform for clinical research and the only chip system approved by the US FDA and China CFDA with EU IVD and CE marks, suitable for RNA and DNA- based clinical detection. Product Coverage of CMA Detection Prenatal detection and diagnosis of chromosomal abnormalities Sample types: Peripheral blood, villi, amniotic fluid, cord blood and abortus It can detect various chromosomal fetal chromosomal abnormalities, including copy number variation (CNV), uniparental diploidy (UPD), loss of heterozygosity (LOH), mosaicism, etc., such as Fancomi anemia or VACTERL syndrome caused by CNV; UPD caused Angelman syndrome, Prader Willi syndrome; and chromosomal abnormalities such as Autism, Cri-du-chat syndrome, Wolf Hirschhorn syndrome, Williams Beuren syndrome, etc. Neonatal genetic disease diagnosis Sample type: Peripheral Blood Precise genetic diagnosis of children with birth defects such as mental retardation, developmental delay, polymorphism, autism, ADHD, epilepsy, neuromuscular disorders, and congenital heart disease Specification of CMA Detection CNV probe 550,000 SNP probe 200,436  Resolution 100kb LOH/UPD ＞5MB For more information about transcriptome sequencing service and in vitro diagnostic assay, please feel free to contact us!

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CapitalBio® Microarray Scanner LuxScan™10K/D, a novel optical system design based on the laser confocal principle, improves detection sensitivity and is suitable for dual-color or single-color fluorescence detection and analysis of high, medium, and low-density biochips. The LuxScan™10K/D optical system works on the laser confocal principle. It increases the sensitivity of detection and can be used for either single-color or dual-color fluorescence detection and analysis of high, medium, or low density biochips. Features of CapitalBio® Microarray Scanner LuxScan™10K/D The first microfluidic in situ fluorescence scanner for detecting amplified nucleic acids Two fluorescence detection channels can be monitored independently due to sequential scanning, and the laser intensity and PMT can be fine-tuned in real- time. LuxScan10K/D has a much larger numerical aperture of 0.76 than the industry standard of 0.68. The amount of light that can be collected is directly related to the lens's numerical aperture. Specification of CapitalBio® Microarray Scanner LuxScan™10K/D Chip size Length (74.85~75.00)mm/ Width(24.85~25.00)mm/Thickness(1.900~2.000)mm< , br>Scan zone ≥22×72mm, equipped with a customized scanning zone Scanner resolution Options include 5um, 10um, 20um, and 40um resolutions. Scan speed ≤30s/cm2 (10um resolution) Sensitivity ≤0.1 fluorescent molecules/um2 Repeatability ≥95%, CV≤10% Weight ≤40kg Dimension (L×W×D) 540mm×360mm×220mm As one of the most professional biotech sequencing companies, we provide genechip scanner, sequencing solutions, etc. For microarray scanner price or more information, please feel free to contact us!

The CapitalBio LuxScan™ 10K dna microarray scanner is a compact high performance system for microarray imaging and the analysis of DNA, protein, and cell arrays. Its advanced systems for optics, signal processing, and motion control provide superior scan accuracy and high detection sensitivity over a wide linear dynamic range. With the optimized signal acquisition and processing elements, it is ideal for profiling high-density spotted microarrays. LuxScan™ 10K-A has two excitation lasers (532nm and 635nm) and scans sequentially, avoiding potential signal crosstalk for dual labeled arrays. LuxScan™ 10K-B comes with either a 532nm or 635nm excitation laser. It has a National Registration Certificate for Medical Devices and is suitable for diagnostic uses. Features And Advantages Of CapitalBio® Microarray Scanner LuxScan™10K Proprietary confocal optical design Sequential scanning, without cross-talk between channels High resolution and high sensitivity Laser intensity and PMT are continuously adjustable Flexibility in dye selection Image quality & signal to noise ratio (SNR) superior to equivalent instruments Remarkably compact, the bench-top footprint of 54 cm × 36 cm Easy-to-use, powerful integrated acquisition, and analysis software - SpotData™ Pro 3.0 with three licenses for each instrument, and free upgrades for the first 5 years LuxScans are available in U.S. standard and European slide formats LuxScan™ 10K Autofocus software allows users easily readjust the altered focus due to rough shipment and for its long term maintenance Specification Of CapitalBio® microarray reader LuxScan™10K Features Parameters cnip Formats: Standard USA Slides (76.2士0.5)×(25.4土0.25)× (1.0土o.1) mm or European slides versions (76.2士0.5)×(25.6土0.25)×(1.0土o.i1) mm Maximum Scan Area 22 mm x 72 mm Excitation wavelength 532 nm and/or 635 nm Emission wavelength 570土10 nm,675土10 nm (expandable to 6 types) Applicable Fluorescence Dyes cy3.cy5, etc. scan Resolution user-selectable: 5,10,20,40 um sensitivity 0.1 chromophores / um2(cpsm)(cy3) scan speed 8 mins / chip (10 um resolution) Dynamic Range 104(16 bit) Repeatability 95% Laser Power settings 5-100 % continuously adjustable PMT Adjustment 450-950 continuously adjustable Focus Distance 土250 um lmage File Format TIFF.BMP, JPG, RAW voltage Ac l1o v/Ac 220v Power 75 watts size (w x D*H) 360 mm x 540 mm x 220 mm (14.2 in x 21.3 in x 8.7 in) weight 40 kg (88 lb) As one of the most professional biotech genetic sequencing companies, we provide protein chip, life sciences instruments, etc. For more information, please feel free to contact us!

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