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BioReagent, for cell culture, sterile, 5.0 mg/mL BioReagent,for Cell culture,Sterile for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Poly-D-lysine (D-type), also known as Poly-D-lysine or abbreviated as PDL. This Poly-D-lysine is Poly-D-lysine hydrobromide, with the molecular formula D-Lys-(D-Lys)n-D-Lys·xHBr, a molecular weight of 150,000–300,000, and CAS Number 27964-99-4.
This product is a ready-to-use Poly-D-lysine solution that has been filter-sterilized. It can be directly diluted for experiments in cell or tissue culture. It is suitable for anti-detachment treatment of slides in histology, immunohistochemistry, frozen sections, cell smears, in situ hybridization, and other experiments to prevent tissue detachment during experimental procedures. It can also be used in cell culture to enhance cell adhesion.
Both Poly-D-lysine and Poly-L-lysine can be used to promote cell adhesion and growth. Poly-L-lysine can be digested and absorbed by certain cells, and excessive intake of Poly-L-lysine may cause some cytotoxicity. If Poly-L-lysine exhibits cytotoxicity in your application, consider using Poly-D-lysine as an alternative.
Instructions for Use
When using Poly-D-lysine for cell-related coating experiments, optimize the coating conditions based on the specific cell line and application.
1.Dilution: Dilute the Poly-D-lysine solution with sterile purified water or PBS to the working concentration, typically 0.1 mg/mL (i.e., 0.01%). This corresponds to a 50-fold dilution of this product to prepare the working solution.
2.Temperature Adjustment: Before use, allow the diluted Poly-D-lysine solution to reach room temperature (18–26°C).
3.Coating:
Culture Vessels (flasks, dishes, plates): Add the working concentration of Poly-D-lysine solution to the culture vessel, with the volume depending on the size of the vessel. Generally, enough solution should be added to cover the growth surface. Incubate at 37°C for 2–4 hours or at room temperature overnight under sterile conditions. Remove the Poly-D-lysine solution and rinse the culture vessel with sterile purified water or PBS. Allow it to dry under sterile airflow in a biosafety cabinet before use. Rinse the vessel once with culture medium before cell seeding, then inoculate cells into the pre-coated vessel.
Slides: Immerse the slides in the working concentration of Poly-D-lysine solution for 5 minutes. Extending the immersion time does not improve coating effectiveness. Dry the slides in a 60°C oven for 1 hour or at room temperature overnight, ensuring sterile handling. Coated slides can be stored at room temperature for up to one year.
Precautions
1.Before coating, slides must be kept clean. If necessary, clean them with a 70% ethanol solution containing 1% HCl.
2.Diluted Poly-D-lysine solution can be stored at 2–8°C and remains stable for at least 3 months.
3.Reuse of diluted solution requires filtration. Discard the solution if it appears turbid or contaminated.
4.For your safety and health, please wear a lab coat and disposable gloves during operation.
| Canonical Smiles | C(CCN)CC(C(=O)O)N.Br |
|---|---|
| IUPAC Name | (2R)-2,6-diaminohexanoic acid;hydrobromide |
| InChIKey | MEXAGTSTSPYCEP-NUBCRITNSA-N |
| INCHI | 1S/C6H14N2O2.BrH/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H/t5-;/m1./s1 |
| Isomeric SMILES | C(CCN)C[C@H](C(=O)O)N.Br |
| PubChem CID | 87493163 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids |
| Direct Parent | D-alpha-amino acids |
| Alternative Parents | Medium-chain fatty acids Amino fatty acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Monoalkylamines Hydrocarbon derivatives Hydrobromides Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | D-alpha-amino acid - Medium-chain fatty acid - Amino fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Hydrobromide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Aug 14, 2026 | P768002 | |
| Certificate of Analysis | Jun 18, 2026 | P768002 |
| Flash Point(°F) | Not applicable |
|---|---|
| Flash Point(°C) | Not applicable |
| 1. Hai-Mu Ye, Shu-Fang Yao. (2017) Supernucleating Role of Poly(ω-pentadecalactone) during the Crystallization of Poly(ε-caprolactone) Composites. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, [PMID:] [10.1021/acs.iecr.7b03322] |
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