Precision-engineered conjugation for antibodies and nanobodies using cysteine re-bridging, enzymatic ligation, and glycan or click chemistries. Achieve homogeneous conjugates, controlled DAR, and LC-MS verified quality under ISO-certified systems.
Bio-Synthesis conjugation services provide advanced site-specific platform enables homogeneous antibody-drug conjugates (ADCs) and nanobody-fluorophore conjugates through bioorthogonal click and enzymatic Sortase A labeling. We combine bis-maleimide re-bridging, enzymatic ligation, glycan-directed oxime/hydrazone, and click chemistry (DBCO↔Azide, TCO↔Tetrazine) to build homogeneous conjugates for ADC prototypes, imaging probes, and nanobody-drug conjugates.
Our linker portfolio (pyridazinedione, dibromomaleimide, Sortase A, TGase, FGE) is verified by LC-MS, HIC, and SEC-MALS under ISO 9001/13485 workflows—improving stability, pharmacokinetics, and reproducibility from discovery to preclinical scale.
Learn more about our antibody conjugation expertise or payload and label conjugation capabilities.
✓ Compatible | △ Conditional (buffer or sequence dependent) | ✗ Avoid
Yes—C-terminal Cys-tags (maleimide), Sortase LPXTG, or click handles (DBCO/azide or TCO/tetrazine) are supported. We deliver site-specific, homogeneous nanobody conjugates for imaging or payload delivery.
Antibody/nanobody identity, buffer & concentration, desired chemistry (re-bridging/enzymatic/glycan/click), target DAR/DoL, QC requirements, and return buffer/format.
Choose re-bridging for DAR≈2 and restored disulfides; choose Sortase/TGase for terminal precision; choose glycan-directed when you need uniform Fc labeling away from CDRs. Click routes enable orthogonal dual payloads.
Intact/subunit LC-MS, HIC for DAR distribution, SEC-MALS for aggregation, and binding (ELISA/SPR/BLI). Optional: release testing for cleavable linkers.
Tell us about your biomolecule, desired label/payload, and intended use. We’ll recommend chemistry, linker design, and release testing to meet your goals.
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