Advanced HLA Typing & Lab Equipment
We supply a comprehensive range of blood transfusion safety Test Kits.
We deliver diagnostic solutions for ensuring safe blood transfusion.
A NGS panel of blood transfusion safety reagents covering:
• ABO blood group typing
• Rare blood group (e.g. Rh, Kell, Duffy, Kidd, MNS) identification
• Human Platelet Antigen (HPA) genotyping / typing
Human Platelet Antibody Typing Kits is coming soon.
Geno Cord Rare Blood Group NGS Typing Kit
Discover the Geno Code Rare Blood Group NGS Kit.
Achieve molecular precision in transfusion safety with comprehensive coverage of rare, weak, and partial blood group antigens.
Product Discription
1. Rare Blood Group NGS Kit
Geno Code Rare Blood Group NGS Kit delivers high-resolution molecular typing for RHD, Kell, Kidd, Duffy, MNS & ultra-rare ISBT systems. Replace serology with certainty.
2. Long-Read / Nanopore Kit
Resolve complex Rh variants with the Geno Code Long-Read Kit. Nanopore-based rare blood group typing for structural variants and repetitive regions missed by short-read NGS.
3. Modular Panel Page
Customize your rare blood group testing. Geno Code modular panels support Rh analysis, antigen screening, and donor matching for transfusion medicine labs worldwide.
Technical Highlights
1.Comprehensive Molecular Coverage
From Common to Ultra-Rare Blood Groups/Core panel covers all major clinically significant systems:
RHD/RHCE, Kell, Kidd, Duffy, MNS, Lutheran, Diego, Dombrock, Colton, Cartwright, Scianna
Optional reflex configurations extend coverage to additional ISBT-recognized rare systems, including:
Vel, JR, Lan, H/Secretor, Lewis, P1PK, Globoside, Landsteiner-Wiener, Xg, Gerbich, Cromer, Knops, Indian, Ok, Raph, JMH, I, Gill, RhAG, FORS, CD59, Augustine, KANNO, Sid, CTL2, PEL, MAM, EMM, Er, ABCC4, CD36, and beyond.
Benefit: One assay replaces multiple serological tests and resolves even the rarest antigenic profiles.
2.Precise Variant Resolution
See What Serology Cannot
Detects common, low-frequency, high-frequency, weak, partial, null, and rare variants; Identifies antigen-defining polymorphisms, silent alleles, and sequence changes affecting antigen expression
Resolves ambiguous or inconclusive serological results with nucleotide-level accuracy
Benefit: Eliminates guesswork in complex cases such as partial Rh antigens or weak D phenotypes.
3.Modular Panel Design
Flexible Configurations for Every Need; Comprehensive Rare Blood Group Profiling – full molecular phenotype; Focused Modules – Rh variant analysis, Kell/Kidd/Duffy/MNS typing
Rare Antigen Screening – rapid identification of antigen-negative donors; Customizable target sets to match laboratory and clinical requirements ;; Scalable from research discovery to routine clinical implementation.
4.Advanced NGS Workflow
High-Throughput, Scalable, Automation-Ready
Targeted PCR enrichment;Indexed library preparation
High-throughput sequencing; Automated genotype-to-predicted phenotype interpretation
Benefit: Seamlessly integrates into existing molecular diagnostics and transfusion medicine workflows.
5.Broad Clinical Utility
Solving Real-World Immunohematology Challenges
Extended blood group typing
Rare donor identification and screening
Donor–patient matching for chronic transfusion recipients
Antibody investigation support
Serologic discrepancy resolution
Molecular confirmation when routine serology fails
Discovery of novel or rare alleles
Benefit: Improves transfusion safety, reduces alloimmunization risk, and supports fetal and neonatal care.
6.Dual-Platform Availability
Short-Read Accuracy + Long-Read Clarity
Optimized for Illumina® and compatible short-read platforms
Geno Code Rare Blood Group Long-Read / Nanopore Typing Kit
Application-Specific
Transfusion Medicine
Improve donor-patient matching and prevent alloimmunization. Geno Code NGS kits enable precise rare blood group typing for safer, personalized transfusion medicine.
2. Rare Donor Screening
Identify rare antigen-negative donors faster. Geno Code NGS panels screen for ultra-rare blood groups, supporting national registries and life-saving transfusions.
3. Serologic Discrepancy Resolution
Resolve inconclusive serology with molecular clarity. Geno Code NGS detects weak, partial, and null alleles causing serologic discrepancies in blood bank testing.
🩸 Geno Code ABO Genotyping Platform
Sequence-Based Solutions for Definitive ABO Blood Group Analysis
Resolve ambiguous serology, characterize rare variants, and enable confident ABO allele assignment across clinical and research applications — from routine transfusion medicine to novel allele discovery.
Why Choose Geno Code?
✔️ Expert-Led Design: Assays built specifically for complex immune gene regions with high polymorphism and structural diversity
✔️ Scalable & Cost-Effective: From single-gene tests to large-scale panels, fit for labs of any size
✔️ Regulatory-Ready: Workflows aligned with clinical and research standards for reproducible, publication-grade results
Contact us to request a quote, sample dat, or custom assay consultation.
Geno Code™ HPA NGS Typing Kit
High‑Resolution Human Platelet Antigen Genotyping by Next‑Generation Sequencing
The Geno Code HPA NGS Typing Kit delivers targeted, amplicon‑based sequencing of clinically relevant HPA polymorphisms (HPA‑1 through HPA‑21). Its modular design supports accurate platelet immunogenetics testing for matched donor selection, FNAIT evaluation, and platelet transfusion investigations.
Key Features
- Comprehensive HPA coverage (HPA‑1 to HPA‑21)
- Detection of allele‑defining polymorphisms & rare variants
- Modular panel design for scalable laboratory testing
- Streamlined NGS workflow with standardized interpretation
Applications
- Platelet donor typing & registry support
- HPA‑matched platelet transfusion strategies
- Platelet transfusion refractoriness investigation
- Fetal & neonatal alloimmune thrombocytopenia (FNAIT)
- Post‑transfusion purpura (PTP) evaluation
- Platelet immunology research
REQUEST DEMO OR MORE INFORMATION
Contact Geno Code
Get in touch
E-mail: info@geno-code.com
whatsapp: +447404914814
Address : Suite G04, 1 Quality Court, Chancery Lane,
London WC2A 1HR, United Kingdom