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52 risultati per Reagenti per estrazione di proteine | Avantor

Reagenti per estrazione di proteine

Reagenti per estrazione di proteine

I reagenti per la purificazione delle proteine vengono utilizzati per isolare una o più proteine da una miscela complessa, solitamente da cellule, tessuti o organismi interi. Questo processo è fondamentale per la caratterizzazione della funzione e della struttura, nonché per identificare le interazioni della proteina di interesse. Durante le varie fasi, i reagenti per la purificazione delle proteine assistono nella lisi cellulare, nella separazione delle componenti proteiche solubili dai detriti cellulari e infine nella separazione della proteina di interesse dalle impurità legate al prodotto e al processo.

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Mass spectrometry reagents, MALDI matrices, single-use

Mass spectrometry reagents, MALDI matrices, single-use

Supplier: Thermo Fisher Scientific

MALDI Matrices are highly purified, recrystallised reagents packaged in convenient single-use tubes sufficient for analysing up to 96 samples.

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Pegylation reagents, methyl-PEG-amine compounds

Pegylation reagents, methyl-PEG-amine compounds

Supplier: Thermo Fisher Scientific

The methyl-PEGn-amine (MA[PEG]n) PEGylation reagents are methyl ether-terminated PEG amines that are used for modifying proteins or surfaces such as beads, nanoparticles and self-assembled monolayers. These PEGylation reagents are homogenous compounds of defined molecular weight and spacer length, providing precision in optimising modification applications.

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MALDI Biotyper® Biotargets

Supplier: BRUKER DALTRONIK

The MBT Biotargets are equipped with hydrophobic coating on the target surrounding the hydrophilic sample positions facilitates the preparation of samples.

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Protein A from Staphylococcus aureus, MP Biomedicals

Supplier: MP Biomedicals

Protein A is a recombinant Fc-binding protein from Staphylococcus aureus, Cowan strain-1 gene. The product is a carboxy truncated material containing 301 amino acid residues. The non-binding regions have been removed to minimise potenial steric interference.

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