1. GPCR/G Protein Neuronal Signaling
  2. CaSR 5-HT Receptor
  3. Poly-D-lysine hydrobromide (MW 150000-300000)

Poly-D-lysine hydrobromide (MW 150000-300000)  (Synonyms: PDLHB (MW 150000-300000))

Cat. No.: HY-139201E
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Poly-D-lysine hydrobromide (MW 150000-300000) is a synthetic polymer composed of D-lysine residues and is one of the most widely used matrices in neural cell culture applications. Poly-D-lysine hydrobromide (MW 150000-300000) can be used as a non-specific cell adhesion enhancer. Poly-D-lysine hydrobromide (MW 30000-70000) is an orally active CaSR agonist peptide that indirectly activates the 5-HT₃ receptor signaling pathway, delaying gastric emptying and thereby slowing the rate at which glucose enters the small intestine and is absorbed.

For research use only. We do not sell to patients.

Poly-D-lysine hydrobromide (MW 150000-300000)

Poly-D-lysine hydrobromide (MW 150000-300000) Chemical Structure

CAS No. : 27964-99-4

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Description

Poly-D-lysine hydrobromide (MW 150000-300000) is a synthetic polymer composed of D-lysine residues and is one of the most widely used matrices in neural cell culture applications. Poly-D-lysine hydrobromide (MW 150000-300000) can be used as a non-specific cell adhesion enhancer. Poly-D-lysine hydrobromide (MW 30000-70000) is an orally active CaSR agonist peptide that indirectly activates the 5-HT₃ receptor signaling pathway, delaying gastric emptying and thereby slowing the rate at which glucose enters the small intestine and is absorbed[1][2].

In Vitro

Poly-D-lysine hydrobromide (0.1 mg/mL,0-24 h) promotes the formation of strong and stable adhesion plaques in primary cultured rat pulmonary artery smooth muscle cells (PASMCs), while restricting their migration ability[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Migration Assay[2]

Cell Line: PASMCs
Concentration: 0.1 mg/mL
Incubation Time: 0, 8, 12, 24 h
Result: Inhibited cell migration.
In Vivo

Poly-D-lysine hydrobromide (MW 30000-70000) (50 mg/kg, i.g or duodenum administration, single dose) reduces the peak blood glucose level after oral glucose administration[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Oral glucose tolerance test (OGTT) and intraperitoneal glucose tolerance test (IPGTT) established in male Sprague-Dawley rats (7 weeks old), weighing 210-230 g[1]
Dosage: 50 mg/kg
Administration: Oral gavage (i.g.) or duodenum administration, single dose
Result: Significantly reduced the peak blood glucose level after oral glucose administration, but had no significant hypoglycemic effect in the intraperitoneal glucose tolerance test (IPGTT).
Delayed the absorption of glucose by slowing down the rate at which food moves from the stomach to the small intestine.
Molecular Weight

150000-300000

Formula

(C6H14N2O2)n.xHBr

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

CNC(CCCCN)C(N[C@@H](CCCCN)C(N[C@H](CCCCN)C(C)=O)=O)=O.[x].Br.[n]

Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
In solvent -80°C 6 months
-20°C 1 month
Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Poly-D-lysine hydrobromide (MW 150000-300000)
Cat. No.:
HY-139201E
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