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Merck

P1524

Sigma-Aldrich

Poly-L-lysine hydrobromide

Poly-L-lysine hydrobromide

suitable for cell culture, Mol wt ≥300,000

Synonim(y):

Bromowodorek homopolimeru L-lizyny

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25 MG
362,00 zł
100 MG
1080,00 zł
500 MG
3430,00 zł
1 G
4970,00 zł

362,00 zł


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25 MG
362,00 zł
100 MG
1080,00 zł
500 MG
3430,00 zł
1 G
4970,00 zł

About This Item

Numer CAS:
Numer MDL:
Kod UNSPSC:
12352209
eCl@ss:
32160406
Identyfikator substancji w PubChem:
NACRES:
NA.26

362,00 zł


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Nazwa produktu

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

Formularz

powder

masa cząsteczkowa

≥300,000

metody

cell culture | mammalian: suitable

kolor

white to off-white

Zastosowanie

cell analysis

temp. przechowywania

−20°C

ciąg 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

Klucz InChI

WBSCNDJQPKSPII-KKUMJFAQSA-N

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Zastosowanie

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[1][2] and to facilitate endocytosis.[2] 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.

Działania biochem./fizjol.

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.

Komponenty

Poly-L-lysine is a positively charged amino acid polymer with approximately one HBr per lysine residue. The hydrobromide allows the poly-L-lysine to be in a crystalline form soluble in water. A small amount of product may be found in the beta structure because the HBr interferes with hydrogen bonding between amino and either the carboxyl groups or N or O containing moieties.

Przestroga

Sterile solutions are stable for up to 2 years when stored at 2-8°C. It should be stored desiccated at -20°C.

Uwaga dotycząca przygotowania

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.

Komentarz do analizy

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

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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)
Iron-oxide labeling and outcome of transplanted mesenchymal stem cells in the infarcted myocardium
Amsalem Y, et al.
Circulation, 116 (2007)
Joshua Guild et al.
Molecular biology of the cell, 28(14), 1975-1983 (2017-05-05)
The spindle is a dynamic structure that changes its architecture and size in response to biochemical and physical cues. For example, a simple physical change, cell confinement, can trigger centrosome separation and increase spindle steady-state length at metaphase. How this
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

Produkty

Kanjiro Miyata (The University of Tokyo, Japan) provides insights on the rational design of polymeric materials for “smart” oligonucleotide delivery.

Humankind has utilized protein materials throughout its existence, starting with the use of materials such as wool and silk for warmth and protection from the elements and continuing with the use of recombinant DNA techniques to synthesize proteins with unique and useful properties.

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