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Key Documents

P1524

Sigma-Aldrich

Poly-L-lysine hydrobromide

suitable for cell culture, Mol wt ≥300,000

Synonyme(s) :

L-Lysine homopolymer hydrobromide

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About This Item

Numéro CAS:
Numéro MDL:
Code UNSPSC :
12352209
eCl@ss :
32160406
ID de substance PubChem :
Nomenclature NACRES :
NA.26

product name

Poly-L-lysine hydrobromide, mol wt ≥300,000

Forme

powder

Poids mol.

≥300,000

Technique(s)

cell culture | mammalian: suitable

Couleur

white to off-white

Application(s)

cell analysis

Température de stockage

−20°C

Chaîne SMILES 

Cl.NCCCCC(N)C(O)=O

InChI

1S/C18H38N6O4/c19-10-4-1-7-13(22)16(25)23-14(8-2-5-11-20)17(26)24-15(18(27)28)9-3-6-12-21/h13-15H,1-12,19-22H2,(H,23,25)(H,24,26)(H,27,28)/t13-,14-,15-/m0/s1

Clé InChI

WBSCNDJQPKSPII-KKUMJFAQSA-N

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Application

Poly-L-lysine polymers can be used in promoting cell adhesion to solid substrates, conjugation to methotrexate for increased drug transport, microencapsulation of islets, cell microencapsulation technology, microarray glass slide coating, and chromosomal preparations. It has also been used as a transfection agent for efficient labeling and to facilitate endocytosis. Lower molecular weight poly-L-lysine (30,000-70,000) is less viscuous in solution, but higher molecular weight versions provide more attachment sites per molecule.

Actions biochimiques/physiologiques

Poly-L-lysine is a nonspecific attachment factor for cells useful in promoting cell adhesion to solid substrates by enhancing electrostatic interaction between negatively charged ions of the cell membrane and the culture surface. When it is absorbed to the cell culture surface, poly-L-lysine functions to increase the number of positively charged sites available for cell binding. With cells that can digest poly-L-lysine, poly-D-lysine should be used as the attachment factor.

Composants

La poly-L-lysine est un polymère d′acide aminé à charge positive, comportant environ un HBr par résidu de lysine. Le bromhydrate permet de former une poudre cristalline de poly-L-lysine soluble dans l′eau. Une petite quantité de produit peut se trouver dans des structures bêta, car le HBr interfère avec la formation de liaisons d′hydrogène entre les groupes aminés et les groupes carboxyliques ou les parties contenant des atomes N ou O.

Attention

Les solutions stériles sont stables pendant environ 2 ans si conservées entre 2 et 8 °C. Conserver à une température de -20  C en présence d′un déshydratant.

Notes préparatoires

Poly-L-lysine hydrobromide has a molecular weight >300,000. To remove the HBr, dissolve this product in a neutral buffer and dialyze to remove the salts. None of the poly-L-lysine products have been exposed to trifluoroacetic acid and are dialyzed to remove any monomers, dimmers, or trimers, confirmed by thin layer chromatography. In general, to use this product as an attachment factor, add 50 mL of sterile tissue culture grade water to 5 mg of poly-lysine, and aseptically coat the surface with 1 mL per 25 cm2 of solution. After 5 minutes, remove the solution through aspiration and thoroughly rinse the surface. Let dry for two hours before introducing cells and medium.

Remarque sur l'analyse

Molecular weight based on viscosity and is also assayed by MALLS.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Miroslaw Janowski et al.
PloS one, 9(2), e97631-e97631 (2014-06-12)
The purpose of the study was to evaluate the long-term clinical tracking of magnetically labeled stem cells after intracerebroventricular transplantation as well as to investigate in vitro feasibility for magnetic guidance of cell therapy within large fluid compartments. After approval
In vivo tracking of mesenchymal stem cells labeled with a novel chitosan-coated superparamagnetic iron oxide nanoparticles using 3.0 T MRI
Reddy AM, et al.
Journal of Korean Medical Science, 25(2), 211-219 (2010)
Takahiro Deguchi et al.
Scientific reports, 6, 22585-22585 (2016-03-05)
To elucidate processes in the osteoclastic bone resorption, visualise resorption and related actin reorganisation, a combination of imaging technologies and an applicable in vitro model is needed. Nanosized bone powder from matching species is deposited on any biocompatible surface in
Lindsay Lewellyn et al.
The Journal of cell biology, 193(1), 155-169 (2011-04-06)
The chromosomal passenger complex (CPC) and centralspindlin are conserved cytokinesis regulators that localize to the spindle midzone, which forms between the separating chromosomes. Previous work placed the CPC and centralspindlin in a linear pathway that governs midzone formation. Using Caenorhabditis
Iron-oxide labeling and outcome of transplanted mesenchymal stem cells in the infarcted myocardium
Amsalem Y, et al.
Circulation, 116 (2007)

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