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440 resultater for "peptide synthesis"

"peptide synthesis"

440 Resultater
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[EN]REACTOR FOR PEPTIDE SYNTHESIS 2ML IN 1 * 10 Items

Supplier: Roth Carl

[EN]REACTOR FOR PEPTIDE SYNTHESIS 2ML IN 1 * 10 Items

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[EN]REACTOR 5 ML FOR PEPTIDE SYNTHESIS 1 * 100 Items

Supplier: Roth Carl

[EN]REACTOR 5 ML FOR PEPTIDE SYNTHESIS 1 * 100 Items

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L(-)-Tyrosin, off-white powder cell culture reagent

Supplier: MP Biomedicals

Storage: Store at room temperature (15-30 °C)
L-Tyrosine is one of the three aromatic amino acids, and is formed from the hydroxylation of phenylalanine.
L-Tyrosine is used in cell culture media and is a component of MEM amino acids solution. L-Tyrosine has been used in a cell culture study of the amino acid transport system b0,+ in epithelial cells isolated from chicken jejunum.

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N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid, HCl, Pierce™

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid, HCl, Pierce™

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

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N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid, HCl, No-Weigh™ Format, Pierce™

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

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[EN]N,N'-DICYCLOHEXYLCARBODIIMIDE (DCC) 1 * 250 g

Supplier: Roth Carl

[EN]N,N'-DICYCLOHEXYLCARBODIIMIDE (DCC) 1 * 250 g

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[EN]SYRINGE REACTORS FOR PEPTIDE SYNTHES 1 * 100 Items

Supplier: Roth Carl

[EN]SYRINGE REACTORS FOR PEPTIDE SYNTHES 1 * 100 Items

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[EN]1-ETHYL-3-(3-DIMETHYLAMINOPROPYL)CAR 1 * 5 g

Supplier: Roth Carl

[EN]1-ETHYL-3-(3-DIMETHYLAMINOPROPYL)CAR 1 * 5 g

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