Empowering Precision in Prenatal Testing！
Discover our advanced NIPT Reference Standards—ensuring the accuracy and safety of every pregnancy journey.
Product Center
CBPJ000-3/6/7/8/11/13/15/17/18
CBPJ000-3/6/7/8/11/13/15/17/18
CBPJ000-1/2/9/10/14/16
CBPJ000-1/2/9/10/14/16
Product Introduce
Our NIPT Reference Standards provide reliable, high-quality solutions for non-invasive prenatal testing. These products cover a broad range of chromosomal aneuploidies, including autosomal and sex chromosomes, as well as microdeletions and microduplications, ensuring comprehensive support for accurate prenatal diagnostics. Each reference standard is rigorously tested to meet the highest standards of precision, empowering laboratories to deliver trustworthy results. With the upcoming introduction of chimeric reference products, CB-Gene continues to lead the way in enhancing the accuracy and safety of NIPT, offering a vital tool for improved prenatal screening.
Product Advantages
Our NIPT Reference Standards are designed to enhance the accuracy, safety, and reliability of prenatal testing.
Comprehensive Coverage
Our products provide a wide range of reference standards, including autosomal aneuploidies, sex chromosome abnormalities, and microdeletions. This ensures comprehensive support for various prenatal testing needs, helping labs deliver reliable diagnostic results.
High Precision and Reliability
Each reference standard is rigorously validated to ensure high accuracy in testing. This level of precision enables laboratories to provide trustworthy results, minimizing errors and improving diagnostic confidence.
Enhanced Safety and Efficiency
With non-invasive testing, our products eliminate the risks associated with traditional invasive methods, offering safer prenatal screening. Laboratories can now achieve more efficient results without compromising patient safety.
Application
Clinical Prenatal Screening
Molecular Diagnostics and Genetic Research
Customizable Testing Solutions
Company Advantage
We stands out with a strong foundation in precision diagnostics and a commitment to high-quality, reliable products
Scientific Quality Management
With our ISO9001 certification, we adhere to a stringent quality management system, ensuring that all our products meet the highest standards of accuracy, stability, and consistency.
Experienced and Skilled Team
Backed by a talented team of experts, we leverage advanced technology and extensive experience to drive innovation in molecular diagnostics, ensuring we stay at the forefront of the industry.
Advanced Laboratories
Our lean laboratories, located in Shanghai and Nanjing, China, are equipped to provide continuous and stable high-quality products, supporting both large-scale production and personalized customer needs.
Comprehensive Product Range
We offer a complete set of reference materials, including SNP, Indel, CNV, Fusion, NIPT, and more, covering a wide array of diagnostic needs and offering customized services for a variety of applications.
Contact Us
We're here to assist you! Whether you have questions about our products, services, or need technical support, our team is ready to provide you with the information you need. Reach out to us today!
FAQs
Related Blogs
TF IHC Quality Controls for Targeted Therapy and Companion Diagnostics
Cobioer Gene provides combined positive and negative TF (Tissue Factor) IHC controls in two formats: FFPE tissue blocks and pre-cut FFPE control slides. The controls are validated by immunohistochemistry for routine quality control of TF IHC assays and companion diagnostic assay development. For Research Use Only.
Read More
PSMA IHC FFPE Controls: Paraffin Blocks vs. Pre-Cut Slides
The format of an IHC control can influence how easily a laboratory develops, validates, and monitors a PSMA staining workflow. While both paraffin blocks and pre-cut slides can be used as FFPE control materials, they support different laboratory needs.
Read More
PSMA IHC Positive and Negative 2-in-1 FFPE Control Standards
Reliable immunohistochemistry depends on more than selecting an antibody against the correct target. Laboratories also need appropriate control materials to evaluate whether the staining result is specific, interpretable, and reproducible.
Read More
ATP7B Reference Standards for Multi-Platform Wilson Disease Assay Validation
For laboratories developing and validating genetic tests for Wilson disease (WD), selecting appropriate ATP7B reference standards is an important part of establishing a controlled and reproducible assay. Wilson disease testing may use Sanger sequencing, quantitative real-time PCR (qPCR), droplet digital PCR (ddPCR), or targeted next-generation sequencing (NGS). Each workflow requires well-characterized genomic DNA reference materials to evaluate analytical performance, monitor run-to-run consistency, and support reliable ATP7B variant detection and genotyping. Suitable ATP7B reference standards should have clearly defined genotypes and variant identities, a relevant sample matrix, compatibility with the intended method, and characteristics aligned with the laboratory's validation plan. This article reviews the principal considerations when selecting ATP7B reference standards for multi-platform Wilson disease assay validation.
Read More
Get Touch With Us
Contact Info
Have questions or need assistance? We're here to help! Reach out to our team, and we'll provide the support you need.
