Define the sequence and research requirement
Scientific services
Custom Peptide Design & Synthesis
A complete model pathway from sequence and feasibility review through synthesis, purification, analytical characterization and project-specific delivery.
Submitting an inquiry does not accept an order or promise inventory, price or delivery.
Technical information
Record at a glance
- Project input
- Sequence or target concept, intended research context, scale and target date
- Design review
- Sequence feasibility, liabilities, termini, modifications and counter-ion strategy
- Scale
- Illustrative model: milligram through multigram research scale
- Purification
- Project-defined target with method and acceptance criterion
- Analytics
- RP-HPLC and mass-spectrometry package; optional tests by written scope
- Presentation
- Bulk or aliquoted; lyophilized where technically appropriate
- Availability
- Proposed capability — feasibility and partner review required
- Catalog number
- SP-LS-SVC-CPS
Project pathway
From brief to documented output.
Review feasibility, modifications and analytical plan
Approve written scope and project checkpoints
Synthesize, purify and characterize
Deliver material and controlled project records
Configurable scope
Project options
- N- and C-terminal modification
- Cyclization and disulfide strategy
- Biotin, fluorescent-label and linker concepts
- Lipidation, PEG and conjugation concepts
- Salt exchange and counter-ion review
- Aliquoting, packaging and storage planning
Written outputs
Expected deliverables
- Feasibility and scope memorandum
- Approved project specification
- Project material where accepted
- HPLC and mass-spectrometry summary
- Certificate or project closeout report
Intended laboratory context
Illustrative applications
- New research-peptide candidates
- Modified or conjugated sequences
- Reference and assay materials
- Milligram-to-multigram research projects
Proposed package
Documentation
- PDFProject specificationSample
- PDFApproved quotation and change recordSample
- PDFAnalytical data packageSample
- PDFFinal project reportSample
Proposed capability. Final feasibility, scale, lead time, testing, facility, partner and quality claims require written technical, Quality, operations and counsel approval.
Start with the scientific brief
Make the scope reviewable.
Reference SP-LS-SVC-CPS and include the sequence, structure or target concept, intended non-clinical use, scale, specification, analytical requirements, format and target date.
Prepare a project inquiry