Kangna Bio's peptide synthesis platform integrates fully automatic peptide synthesis, advanced microwave technology and peptide chain extension technology, and can flexibly select liquid phase peptide synthesis (LPPS) or solid phase peptide synthesis (SPPS) according to the sequence. The synthesis platform combined with the fully automatic synthesizer can not only guarantee a monthly synthesis throughput of up to 12,000, but also ensure batch stability between peptide products, with a single synthesis success rate of up to 98%.
Support synthesis range: wide length range (2-200aa), complex modified peptides (phosphorylation/glycosylation/fluorescence labeling, etc.)
Detection Dimension |
Technical means |
Quality Control Standards |
Purity analysis |
HPLC/UPLC |
≥95% conventional quality control |
Molecular weight verification |
MALDI-TOF/MS |
Error<0.1% |
Biological Activity |
Cell assay/ELISA |
Batch-to-batch variation <5% |
stability |
Accelerated experiment/long-term sample retention |
Comply with ICH guidelines |
Application Areas |
Representative Products |
Targeted therapy |
iRGD tumor-penetrating peptide, GLP-1 analog (liraglutide), angiotensin derivatives |
Anti-infective agents |
Polymyxin B sulfate, human defensin HNP-1, daptomycin custom modifications |
Diagnostic reagent development |
FITC labeled peptides, isotope (125I) labeled peptides, biotin-avidin system modified peptides |
Innovative raw materials for medical beauty |
Palmitoyl hexapeptide-12 (promoting collagen), copper tripeptide GHK-Cu (repair), acetyl tetrapeptide-2 (anti-wrinkle) |
Submission method: Official website work order/technical consultant connection
Key elements:
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*Company/Organization Name: |
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*Peptide Name: |
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CAS No.: |
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Peptide salt form: |
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Peptide sequence |
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N-terminal modification type: |
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C-terminal modification type: |
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Other modifications: |
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Disulfide bonds: |
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Solubility Test: |
DMSO/DMF ( ) H2O ( ) Other solvents ( ) |
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Molecular simulation: conformational analysis using MOE software
Synthesis route: segmented strategy optimization (modular synthesis is used for peptides >30aa)
Risk assessment: prediction of difficult sites (such as multiple consecutive hydrophobic amino acids)
Cycle management: conventional peptides (5-15 working days), complex modified peptides (15-30 working days)
Process monitoring: staged HPLC detection (crude product → purification → freeze-drying)
Delivery standard: complete analysis report (including MS, HPLC spectrum, COA document)
Professional support: Synthesis team led by a PhD
Equipment support: ABI Symphony® fully automatic synthesizer, Waters UPLC and other cutting-edge equipment
Storage and transportation: -20℃ cold chain transportation