Esta buscando: N-Acetyl-D-phenylalanine

Proveedor: TCI

Descripción: Biotin hydrazide ≥98.0% (by HPLC)

Numero del catalogo: (APOSBIB108-100MG)

Proveedor: Apollo Scientific

Descripción: Carbohydrate reactive. Microscopy studies on membranesRef: O'Shannessy,D.J.et al. (1984) Immun.Letters 8,273-277

UOM: 1 * 100 mg

Promoción

Proveedor: Cayman Chemical

Descripción: Biotin hydrazide is a biotinyl derivative used to label surface functional groups, antibodies, lectins, sugars, nucleic acids, or molecules with free carboxylic or keto groups.

Numero del catalogo: (APOSBIB109-100MG)

Proveedor: Apollo Scientific

Descripción: Carbohydrate reactive -Spacer armMore sensitive than biotin hydrazide.

UOM: 1 * 100 mg

Promoción

Proveedor: TCI

Descripción: Biotin-PEG4-hydrazide 94,0 HPLC_ASSAY_METHOD

Proveedor: TCI

Descripción: Biotin-LC-hydrazide 97,0 HPLC_ASSAY_METHOD

Proveedor: Biotium

Descripción: Biotium offers reactive biotin compounds with a variety of reactive functional groups.

Numero del catalogo: (AATB3007)

Proveedor: AAT BIOQUEST

Descripción: Biotin and biotin derivatives bind with high affinity to both avidins and streptavidins.

UOM: 1 * 25 mg

Promoción

Numero del catalogo: (AATB3055)

Proveedor: AAT BIOQUEST

Descripción: Biotin/avidin complexes are widely applied for a variety of biological detections.

UOM: 1 * 5 mg

Promoción

Proveedor: G-Biosciences

Descripción: HOOK™ Biotin-Hydrazide and its long spacer arm equivalent, HOOK™ Biotin-LC-Hydrazide, are carbohydrate reactive reagents. HOOK™ carbohydrate reactive biotin reagents react with oxidised carbohydrate side chains. Some biotin reagents do not bind directly to the protein itself, but instead, conjugate to the carbohydrate residues of glycoproteins. The carbohydrate reactive biotin reagents contain hydrazides (-NH-NH₂) as a reactive group. The hydrazide reactions require carbonyl groups, such as aldehydes and ketones, which are formed by oxidative treatment of the carbohydrates. Hydrazides react spontaneously with carbonyl groups, forming a stable hydrazone bond. These reagents are particularly suitable for labelling and studying glycosylated proteins, such as antibodies and receptors.

Proveedor: Thermo Fisher Scientific

Descripción: A common target for protein modification is the carbohydrate portion of glycoproteins, which can be reacted with hydrazide derivatives of biotin. Oxidative treatment of glycoproteins using 10 mM periodate is used to generate reactive aldehydes from the cis-diols of a variety of carbohydrate moieties.

Proveedor: G-Biosciences

Descripción: HOOK™ Biotin Reagent that conjugates to proteins through amines, sulfhydryls, carboxyls or carbohydrates. The amine and sulfhydryl coupling HOOK™ Biotin Reagents couple directly to the protein through their reactive groups, however the carboxyl coupling HOOK™ Biotin Reagents require a carbodiimide crosslinker and the carbohydrate coupling HOOK™ Biotin Reagents require carbohydrate oxidation before coupling.

Proveedor: G-Biosciences

Descripción: HOOK™ Biotin-PEG₂-Amine, and its long chain form, HOOK™ Biotin-PEG₃-Amine, are carboxyl reactive biotinylation reagents. These agents contain terminal amines and react with carboxyl groups found at the carboxyl termini, aspartate, and glutamate side chains. The reaction is mediated by a water-soluble carbodiimide (EDC). The carbodiimide activates the carboxyl group and reacts with the amines (-NH₂) on the biotinylation agent to form an amide bond. This reaction is rapid and takes just a few minutes to complete. Under these conditions, hydrazide-derivatives of biotin reagents may also react with the carboxyls.

Numero del catalogo: (TCIAT1820-25G)

Proveedor: TCI

Descripción: L-Tyrosine hydrazide 98,0 HPLC, T

UOM: 1 * 25 g

Promoción

Proveedor: TCI

Descripción: Methylmaleic hydrazide 98,0 GC_ASSAY_METHOD

Numero del catalogo: (TCIAO0156-5G)

Proveedor: TCI

Descripción: Oxamic hydrazide ≥95.0% (by titrimetric analysis)

UOM: 1 * 5 g

Promoción