You Searched For: H-N-Me-Ala-OMe·HCl


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Supplier: MP Biomedicals
Description: MES is a zwitterionic buffer.

Supplier: Merck
Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: MP Biomedicals
Description: Solubility (5% aq soln) clear, colorless solution.

Supplier: Merck
Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®
Supplier: Merck
Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Catalog Number: (AATB13479)
Supplier: AAT BIOQUEST
Description: The weakly fluorescent AMC substrates generate the bright blue fluorescent AMC product that has Ex/Em = 351/430 nm, and can be easily detected with a DAPI filter set.
UOM: 1 * 5 mg


Supplier: Merck
Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: Avantor
Description: Buffer for liquid chromatography and other molecular biology applications. Lot analysis on label.
Supplier: Merck
Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: Merck
Description: Glycinamide hydrochloride (H-Gly-NH2.HCl), Sigma-Aldrich®

Supplier: Apollo Scientific
Description: Used in the reduction of disulphide groups.

Catalog Number: (CAYM14329-1)
Supplier: Cayman Chemical
Description: TCEP-HCl (Tris(2-carboxyethyl)phosphine hydrochloride)
UOM: 1 * 1 g


Supplier: Merck
Description: Glycinamide hydrochloride (H-Gly-NH2.HCl), Sigma-Aldrich®

Supplier: Thermo Fisher Scientific
Description: 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.
Catalog Number: (SIAL75259-1G)
Supplier: Merck
Description: TCEP-HCl (Tris(2-carboxyethyl)phosphine hydrochloride), Sigma-Aldrich®
UOM: 1 * 1 g


Supplier: Thermo Fisher Scientific
Description: TCEP-HCl (Tris(2-carboxyethyl)phosphine hydrochloride) 98% for molecular biology
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
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