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Merck

A-003-M

Poly-ᴅ-Lysine Hydrobromide

synthetic, liquid, 1 mg/mL, suitable for cell culture

Sinónimos:

poly lysine

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UNSPSC Code:
12352207
eCl@ss:
32160801
NACRES:
NA.75
Biological source:
synthetic
Form:
liquid
Technique(s):
cell culture | mammalian: suitable
Servicio técnico
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Nombre del producto

Poly-D-Lysine solution, 1.0 mg/mL, The Poly-D-Lysine solution promotes the adhesion of tissues/sections to the culture vessel.

biological source

synthetic

Quality Level

form

liquid

manufacturer/tradename

Specialty Media

technique(s)

cell culture | mammalian: suitable

input

sample type neural stem cell(s)
sample type epithelial cells
sample type: human embryonic stem cell(s)
sample type hematopoietic stem cell(s)
sample type mesenchymal stem cell(s)
sample type pancreatic stem cell(s)
sample type induced pluripotent stem cell(s)

General description

Poly - D Lysine (PDL), a chiral form of alpha polylysine is a synthetically produced cationic polypeptide. It is a non-specific cell adhesion molecule (CAM). PDL is used extensively as a coating material in in vitro and ex vivo experiments.

Application

Poly-D-Lysine has been used:
  • To coat culture vessels and provide a suitable surface for the growth and attachment of neuronal cells.
  • In preparing the surface of coverslips for facilitating the attachment of non-adherent cells.

Biochem/physiol Actions

Poly-D Lysine, (PDL) being cationic, facilitates the interaction with anionic sites on the tissues/cells promoting effective attachment to the growing surface. Positively charged PDL interacts with negatively charged cell membranes and promotes neurite outgrowth. Covalently bound PDL layers promote long-term culture of neuronal cells.

Features and Benefits

  • Poly-D-Lysine (PDL) solution is diluted in phosphate buffer saline (PBS), water, or 0.1M borate buffer.
  • Working dilutions of 50μg/mL to 100μg/mL are usually adequate.
  • It has a surface coverage of 3-10μg/cm2.
  • PDL can be stored at -20 ˚C for up to 18 months.
  • Plates are coated for 3 hours overnight and up to 3 days when stored at 4˚C.
  • PDL-coated plates are used immediately or stored in PBS for up to 5 days.

Physical form

Liquid. 20ml in sterile water.

Preparation Note

Store at -20C for upto 18 months.
The level of coating will vary for different species and types of cells. In general final coating concentrations from 3-10μg/cm2 of surface area will typically supply sufficient coatings for most cell types. Surface area of plates: (pi)(Radius squared) in cm2 In practical terms working dilutions of 50μg/mL to 100μg/mL are usually adequate. Dilute poly-D-lysine in PBS, water, or 0.1M borate buffer {prepared by adding 1.24 g boric acid and 1.9 g sodium tetraborate in 400 ml water, pH 8.5} to final working concentration. Plates or flasks are coated for 3 hours to overnight, and up to 3 days if stored at 4C. The best results are usually with just overnight coatings. Remove the poly-d-lysine solution and rinse with sterile PBS or water 1-2X. Do not scrape the bottom of the coated plates or flasks. Use plates immediately or store them with PBS for up to 5 days. Poly-D-lysine coating methods will vary slightly from laboratory to laboratory, please use the method as a general guide.


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Clase de almacenamiento

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable



Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Enhancement of neuronal cell adhesion by covalent binding of poly-D-lysine
Hee Kim Y, et al.
Journal of Neuroscience Methods, 202(1), 38-44 (2011)
Evaluation and Optimization of Poly-d-Lysine as a Non-Natural Cationic Polypeptide for Gene Transfer in Neuroblastoma Cells
Sanchez-Martos M, et al.
Nanomaterials (Basel, Switzerland), 11(7), 1756-1756 (2021)
Characterization of Seeding Conditions for Studies on Differentiation Patterns of Subventricular Zone Derived Neurospheres
Sanchez-Mendoza EH, et al.
Frontiers in Cellular Neuroscience (2016)



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SKUGTIN
A-003-E04053252475139