Poly-D-lysine hydrobromide (MW 30000-70000)
CAS No. 27964-99-4
Poly-D-lysine hydrobromide (MW 30000-70000)( —— )
Catalog No. M35204 CAS No. 27964-99-4
Poly-D-lysine hydrobromide (MW 30000-70000) (Poly-D-lysine HBr) is an oral peptide CaSR agonist that eliminates proteinase K-resistant PrP from prion-infected SN56 neuroblastoma cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 29 | Get Quote |
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| 10MG | 46 | Get Quote |
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| 25MG | 90 | Get Quote |
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| 50MG | 144 | Get Quote |
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| 100MG | 205 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
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Biological Information
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Product NamePoly-D-lysine hydrobromide (MW 30000-70000)
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NoteResearch use only, not for human use.
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Brief DescriptionPoly-D-lysine hydrobromide (MW 30000-70000) (Poly-D-lysine HBr) is an oral peptide CaSR agonist that eliminates proteinase K-resistant PrP from prion-infected SN56 neuroblastoma cells.
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DescriptionPoly-D-lysine hydrobromide (MW 30000-70000) is a synthetic polymeric substrate and is one of the most widely used substrate in neural cell culture. Poly-D-lysine hydrobromide (MW 30000-70000) removes proteinase K-resistant PrP from prion-infected SN56 neuroblastoma cells without affecting PrPC.
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In VitroPoly-D-lysine is immunogenic in rabbits only when injected at low doses.The approximate concentration of Poly-D-lysine (PDL) needed to lower the amount of PrPres by 50% corresponds to ~0.8 μg/mL or 50 nM.
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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TargetCaSR
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RecptorCaSR
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Research Area——
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Indication——
Chemical Information
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CAS Number27964-99-4
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Formula Weight
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Molecular Formula(C6H14N2O2)x.xHBr
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 50 mg/mL (Ultrasonic))
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SMILES(C6H14N2O2)x.xHBr
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. HansVermeersch, et al. Immunogenicity of poly-D-lysine, a potential polymeric drug carrier. Journal of Controlled Release. Volume 32, Issue 3, 1 December 1994, Pages 225-229.
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