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Key Documents

767700

Sigma-Aldrich

Mytilus edulis foot protein-1

1 mg/mL (in 1% citric acid), sterile

Sinonimo/i:

MAPcell

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Codice UNSPSC:
12162002
NACRES:
NA.23

Forma fisica

liquid

Concentrazione

1 mg/mL (in 1% citric acid)

Indice di rifrazione

n20/D 1.335 (lit.)

P. eboll.

100-103 °C/760 mmHg

Densità

1.008 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

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Applicazioni

A solution of MEFP-1 that is specially developed for biological applications. The protein can be used to coat surfaces in order to facilitate immobilization of cells and tissue. The solution is sterile by autoclaving and has an endotoxin level of = 1 EU/ml. The product is cell culture tested (cytotoxicity and cell adhesion assay).

MEFP-1 can be successfully used for unspecific immobilization of cells and tissue to essentially any surface. It is an especially useful tool when the surface chemistry results in poor adhesion of cells or for cells that are difficult to attach. In comparison to binding strategies based on electrostatic interactions (positively charged surfaces) or covalent immobilization (EDC/NHS or glutaraldehyde) attachment using MEFP-1 is insensitive to ionic strength and pH and will not result in undesired chemical modification, such as cross-linking, of cell surface components. The protein coating is a useful tool in techniques such as in situ hybridization, immunohistochemistry, tissue engineering, drug delivery, ELISA, microfluidics, microinjection and various microscopy techniques.

Compatibilità

MAPcell is sterile and suitable for cell culture.

Classe di pericolosità dell'acqua (WGK)

WGK 3


Certificati d'analisi (COA)

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J H Waite et al.
Science (New York, N.Y.), 212(4498), 1038-1040 (1981-05-29)
The fouling marine mussel Mytilus edulis attaches itself to various substrates by spinning byssal threads, the adhesive discs of which are rich in the amino acid 3,4-dihydroxyphenylalanine (dopa). An acid-soluble protein was extracted and purified from the phenol gland located

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