



Service | Length | Quantity | Type | Purification | Modification | Conjugation |
---|---|---|---|---|---|---|
siRNA | 20-30nt | 5 nmol to Kg level |
|
RNase free HPLC, desalt | Locked Nucleic Acid (LNA), thioate, methylation, 2-Ome etc. (~200 types) | Antibody, peptide, lipid etc. |
ASO | 15-30nt |
|
QC Item | Test Method | Specification | Standard QC | Customized QC |
---|---|---|---|---|
Appearance | Visual Inspect | White to pale yellow powder | ||
Identity by MW | Mass Spectrometry | Theoretical Average MW ± 0.1% | ||
LC-MS | Liquid chromatography–mass spectrometry | Report result | ||
LC MS/MS Sequencing | High-resolution Mass Spectrometry Sequencing | 100% sequence coverage | ||
Purity by HPLC | High Performance Liquid Chromatography | double-strand siRNA ≥ 90% | ||
Purity by CGE | Capillary Gel Electrophoresis | Report result | ||
Purity by PAGE | Polyacrylamide Gel Electrophoresis | Report result | ||
pH Measurement | Micro pH Electrode Method | Report result | ||
TEA Salt residue detection | Gas chromatography-mass spectrometry Measurement | Report result | ||
Solvent residue | Gas chromatography-mass spectrometry Measurement | Report result | ||
Endotoxin | Chromogenic Method | Report result | ||
Bacterial Testing | Direct Inoculation /membrane filter method | Report result |
Please find more customized QC information in Oligo Quality Control Service>>.
siRNA Negative Control (Scramble sequence) Design Tool
* GenScript offers a free siRNA design tool utilizing classic design logic. If you prefer an AI-enhanced design platform, please choose the siRNA guarantee package or send a request to oligo@genscript.com.
20 nt double-stranded siRNA with 29 2'-O-Methyl modifications, 3 phosphate groups, 13 2'-Fluoro modifications, and 1 GalNAc modification, exhibited purity up to 96.55%
Genscript's Small Nucleic Acid Drugs AI Design Platform
siRNA sequences designed for Gene B with GenScript's bioinformatic design platform achieved higher knockdown efficiency (KD%) than those created with other vendors' tools.
Method: For different modification schemes, the metabolic rate and metabolites in a serum environment were analyzed to select the most stable modification schemes for subsequent optimization and development.
Results
Guarantees Knockdown Efficiency ≥80%
Learn MoreFrom Design to Therapeutic Candidate in 6 Weeks
Learn MoreObtain Candidates with Higher Stability
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