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ผู้นำนวัตกรรมด้านพันธุศาสตร์
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DNA Genetic Cancer Risk Test
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Everyone inherits genetic mutations from their parents. Some inherited mutations can greatly increase the risk of cancer. Rapidy DNA Genetic Cancer Risk Testing can helps you understand your personal risk of inherited cancer.

ทุกคนมีการกลายพันธุ์ของยีน (Mutation) ที่ได้รับถ่ายทอดจากพันธุกรรมต่างกัน ซึ่งหลาย Mutation เป็นสาเหตุในการเพิ่มความเสี่ยงโรคมะเร็ง Rapidy DNA Genetic Cancer Risk Test จึงเป็นบริการตรวจ Mutation ที่จะช่วยให้คุณเข้าใจความเสี่ยงของตนเองมากขึ้น ตรวจ 1 ครั้ง ครอบคลุมกว่า 98 ยีน 25 มะเร็ง

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DNA FISH Probe FDA Approved
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⚬ DNA FISH Probe for Oncology

⚬ DNA FISH Probe for Hematological Cancer
⚬ FISH Reagent

⚬ Thermobrite

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Primary Antibody Automation
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⚬ Xmatrix Infinity

⚬ Xmatrix Mini

⚬ Xmatrix Nano

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Digital Microscopy and Software
for Pathology and Cytogenetics
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⚬ High Throughput

⚬ Capture and Analysis

⚬ Scan and Analysis

⚬ Spectral Imaging

⚬ Review and Analysis

⚬ Data Management

⚬ Genesis Anywhere

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Molecular Diagnostic Products
for Real Time PCR
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⚬ Super-ARMS EGFR Mutations Detection Kit

⚬ KRAS Mutations Detection Kit

⚬ KRAS / NRAS Mutations Detection Kit

⚬ KRAS / NRAS / BRAF Mutations Detection Kit

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SOPHIA GENETICS HEREDITARY
CANCER SOLUTION
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Bundle test : Detection Kit for NGS + Bioinformatics
Only Bioinformatics

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Devyser Complete QF-PCR
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Devyser Complete enables rapid prenatal aneuploidy detection of chromosomes 13, 18, 21 and XY using 33 genetic markers in two separate PCR mixes. Cross mix ID markers are included in both mixes to reduce the risk of sample mix-up. In addition to detecting Down, Edwards, Patau and Klinefelter syndromes, the Devyser Complete kit includes our patented technology for reliable diagnosis of Turner syndrome, using two dedicated X-chromosome counting markers.

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ABBOTT VYSIS
INTELLIFISH SOLUTION
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Enables one-shift FISH with equal or improved quality of results with: Novel chemistry
Reduced hybridization time (2 hours)

The new Vysis IntelliFISH redefines FISH testing with smart features designed to improve lab efficiency while delivering quality results that your customers can count on. FISH becomes EASIER, FASTER, SMARTER.

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LUCENCE
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- LiquidHALLMARK
- LiquidMARK
- Tissue

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Macrogen BABY CARE
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- FAMPLAN is a preconception cerrier screening to aid healthy family planning by predicting the genetic rick to future children by analyzing the parents' genomes.

- NIPS by FAEST is a screening test to detect fetal aneuploidies with NGS analysis of ctDNA from pregnant women's peripheral blood. It is called NIPS since it only needs to analyze the maternal blood sample, avoiding invasive collection of fetal samples that is necessary in cases of the amniocentesis or CVS.

- ABOOBA detects genetic disorders for newborn babies based on whole genome sequencing, leading to more accurate result compared to other platforms being used for newborn screening

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AXEN
Macrogen BRCA1/2
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Macrogen BRCA1/2 testing is a next-generation sequencing test that searches for mutation in BRCA1 and BRCA2 genes. It is best suited for individuals with either a history of early onset breast or ovarian cancer or a strong family history of breast and/or ovarian cancer.

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Address

BCC MDx Co., Ltd.
99 Ratchada-Ramintra Road, Nuanchan, Buengkum, Bangkok 10230 Thailand

Tel 02-010-1599
Fax 02-010-1599

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