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Key Documents

P6516

Sigma-Aldrich

Poly-L-lysine hydrobromide

greener alternative

suitable for cell culture, Mol wt ≤15,000 by MALLS

Synonyme(s) :

L-Lysine homopolymer hydrobromide

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About This Item

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

product name

Poly-L-lysine hydrobromide, mol wt 4,000-15,000 by viscosity

Forme

solid

Poids mol.

≤15,000 by MALLS
4,000-15,000 by viscosity

Score du produit alternatif plus écologique

old score: 51
new score: 43
Find out more about DOZN™ Scoring

Caractéristiques du produit alternatif plus écologique

Designing Safer Chemicals
Safer Solvents and Auxiliaries
Reduce Derivatives
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Technique(s)

cell culture | mammalian: suitable

Couleur

white to off-white

Application(s)

cell analysis

Autre catégorie plus écologique

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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Description générale

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Designing Safer Chemicals”, "Safer Solvents and Auxiliaries" and “Reduce Derivatives”. Click here to view its DOZN scorecard.

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. 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. Poly-L-lysine hydrobromide has been used:
  • as a component of polyplexes and in DNA condensation experiments
  • for coating circular mica disks for atomic force microscopy studies and SuperFrost glass slides for immunofluorescence studies of in HL-60 cells
  • as a reference standard for generating calibration curve for the quantification of ε- Poly-L-lysine

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

This product has a molecular weight of 4,000-15,000. 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.

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

AFM imaging of bacteria in liquid media immobilized on gelatin coated mica surfaces
Doktycz MJ, et al.
Ultramicroscopy, 97(1-4), 209-216 (2003)
Epsilon-Polylysine Fermentation and its Recovery Using Carboxymethyl Cellulose (CMC)-Conjugated Magnetite
Wibowo N, et al.
Separation Science and Technology, 48(7), 1086-1092 (2013)
DNA condensation by poly-L-lysine at the single molecule level: role of DNA concentration and polymer length
Mann A, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society, 125(3), 252-262 (2008)
Retinoic acid differentiation of HL-60 cells promotes cytoskeletal polarization
Olins AL, et al.
Experimental Cell Research, 254(1), 130-142 (2000)
Miaomiao Li et al.
Genome biology, 19(1), 69-69 (2018-06-02)
N 6 -methyladenosine (m6A) modification in mRNAs was recently shown to be dynamically regulated, indicating a pivotal role in multiple developmental processes. Most recently, it was shown that the Mettl3-Mettl14 writer complex of this mark is required for the temporal

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