"peptide synthesis"
[EN]REACTOR FOR PEPTIDE SYNTHESIS 2ML IN 1 * 10 Items
Supplier: Roth Carl
[EN]REACTOR FOR PEPTIDE SYNTHESIS 2ML IN 1 * 10 Items
Expand 1 Items
[EN]REACTOR 5 ML FOR PEPTIDE SYNTHESIS 1 * 100 Items
Supplier: Roth Carl
[EN]REACTOR 5 ML FOR PEPTIDE SYNTHESIS 1 * 100 Items
Expand 1 Items
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.
Expand 3 Items
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.
Expand 3 Items
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.
Expand 1 Items
[EN]N,N'-DICYCLOHEXYLCARBODIIMIDE (DCC) 1 * 250 g
Supplier: Roth Carl
[EN]N,N'-DICYCLOHEXYLCARBODIIMIDE (DCC) 1 * 250 g
Expand 1 Items
[EN]SYRINGE REACTORS FOR PEPTIDE SYNTHES 1 * 100 Items
Supplier: Roth Carl
[EN]SYRINGE REACTORS FOR PEPTIDE SYNTHES 1 * 100 Items
Expand 1 Items
[EN]1-ETHYL-3-(3-DIMETHYLAMINOPROPYL)CAR 1 * 5 g
Supplier: Roth Carl
[EN]1-ETHYL-3-(3-DIMETHYLAMINOPROPYL)CAR 1 * 5 g
Expand 1 Items
Recommendations will be personalized based on your shopping preferences only if you have given your consent by enabling "Enhance my Shopping Experience" on the "Personal Info page".
Otherwise, you will receive generic recommendations.



