From target identification and recombinant enzyme engineering to ultra-pure reagents and automated cell sorting, Synthex equips principal investigators, clinical research facilities, and biotechnology leaders with research-grade and cGMP-certified precision tools.
Proprietary Cas12a ultra-fidelity variants offering single-digit off-target profiles for translational therapeutics research.
Streamlined access to research essentials, certified standards, and production-scale biologicals.
Polymerases, dNTPs & NGS Library Kits
Monoclonal, ELISA & Flow Cytometry
Defined Media, ECM & Primary Lines
HPLC Columns, Resins & Solvents
Liquid Handlers, Bioreactors & Optics
Peptides, Oligos & Bulk Fermentation
Engineered to support translational discovery from early discovery target identification to scalable cGMP production pipelines.
High-fidelity polymerases, long-read NGS library preparation systems, Cas12a/Cas9 ribonucleoprotein complexes, and synthetic oligonucleotides.
Monoclonal antibodies with recombinant epitope validation, mass spectrometry isotopically labeled standards, and cryo-EM grid matrices.
Chemically defined serum-free stem cell media, 3D hydrogel extracellular scaffolds, flow cytometry panels, and primary validated human cell models.
Single-use bioreactor assemblies, scalable filtration membranes, USP grade cell feed supplements, and in-line process analytical technologies (PAT).
IVD control matrices, multiplex immunoassays, point-of-care nitrocellulose membranes, lateral flow beads, and pathogen reference panels.
Sub-2-micron UHPLC columns, certified ACS/Reagent grade solvents, spectrophotometry microplates, and automated pipetting workstation modules.
Our PhD applications scientists provide cross-domain experimental design consultations.
Engineered for structural biology, metabolomics, and ultra-trace impurity characterization with certified compliance for 21 CFR Part 11 regulated labs.
Ultra-high mass resolution exceeding 480,000 FWHM with sub-ppm mass accuracy. Built-in electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) quick-swap modules.
Engineered for extreme operating pressures up to 22,000 psi (1,500 bar). Features cooled multi-well autosamplers and diode array detection (DAD) with zero carryover active wash needles.
Designed for atomic-resolution single-particle analysis and cryo-electron tomography. Automated cassette autoloader with integrated direct electron detector for macromolecular complexes.
Comprehensive compliance certification by factory-certified engineers.
Real-time remote diagnostics and consumable life-cycle tracking.
Guaranteed 24-hour on-site response and loaner hardware availability.
Structured workflow workshops for principal investigators and staff.
Engineered for batch-to-batch consistency. Tested for zero DNase, RNase, and endotoxin contamination to eliminate experimental variation.
50x fidelity of standard Taq. Optimized for difficult GC-rich amplicons up to 12kb. Includes dye-free electrophoresis tracker.
Feeder-free, human stem cell expansion matrix. High pluripotency maintenance over 25+ passages without weekend feeding cycles.
Ultra-hydrophobic medical polymer. Aerosol hydrophobic barrier filter. Fully validated for Tecan, Hamilton, and Agilent platforms.
Simultaneous quantification of IL-6, TNF-alpha, IFN-gamma, and 9 key inflammatory targets. Sub-picogram per milliliter sensitivity.
Lock in identical lots for up to 24 months to protect long-term longitudinal study reproducibility. Automated ERP integration for EDI/PunchOut orders.
From initial lead molecule identification to cGMP commercial fill-finish. Synthex integrates certified hardware, reagent systems, and regulatory validation dossiers at every milestone.
High-throughput CRISPR/Cas knockout libraries, recombinant antibody phage display, and sub-nanomolar affinity validation using surface plasmon resonance (SPR).
High-titer CHO/HEK293 clone stabilization, chemically defined animal origin-free (AOF) feeds, and scalable perfusion bioreactors from 250 mL to 2,000 L.
Protein A affinity resins with alkali-tolerance, viral clearance membrane filtration, tangental flow ultrafiltration cassettes, and excipient stabilization.
21 CFR Part 11 compliant release analytics. Intact mass confirmation via LC-MS, residual host-cell protein (HCP) ELISAs, and recombinant sterility assays.
All Synthex bioprocessing inputs include complete Drug Master Files (DMF) filed directly with the US FDA, EMA, and PMDA to accelerate regulatory filing timelines by up to 6 months.
Peer-reviewed technical whitepapers, step-by-step wet lab protocols, and certified continuing education training modules curated by senior application scientists.
A comprehensive benchmarking of novel hot-start engineered polymerases across 78% GC loci in clinical oncogene panels.
Optimized protocol yielding >94% post-thaw cell viability using defined recombinant matrices without animal serum additives.
Learn chromatographic gradient optimization, solvent modifier selection, and data-independent acquisition (DIA) parameter tuning.
Interactive self-paced training module covering audit trails, electronic signature hygiene, and out-of-specification investigations.
Submit your experimental data or chromatographic traces for review by our senior technical desk.
Connect fragmented laboratory hardware into a synchronized ecosystem. Synthex OS bridges high-throughput liquid handling, real-time sensor streams, and audit-ready data pipelines.
Eliminate pipetting variability and technician fatigue. Modular multichannel heads dispense nanoliter to microliter volumes with automated tip loading, barcode validation, and active liquid level sensing (cLLD).
Non-invasive smart dongles connect legacy centrifuges, -80°C freezers, incubator CO2 levels, and analytical balances to an encrypted telemetry dashboard with automated anomaly dispatch.
Eliminate paper records with end-to-end sample chain-of-custody, raw analytical file parsing, automated standard curve regressions, and cryptographic e-signatures with zero vendor lock-in.
Integrate Python and R computational notebooks directly to auto-trigger physical pipetting routines.
Maximize laboratory uptime, pass regulatory audits effortlessly, and secure bulk institutional pricing with dedicated technical and procurement teams.
Complete on-site verification protocol execution with certified traceability, calibrated test instrumentation, and audit-ready binders signed by certified field service engineers (FSEs).
Guaranteed 24-hour on-site dispatch, bi-annual preventive maintenance overhauls, emergency loaner equipment availability, and all OEM wear-and-tear components included.
Dedicated institutional account executives, automated EDI 850/855/810 invoice transactions, custom Lot Reservations, and cold-chain drop shipments directly to your bench.
Guaranteed quote or technical response within 4 operational business hours.
🔒 All scientific queries and technical data transfers are protected under strict laboratory confidentiality protocols.