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Fornitore: TCI EUROPE
Descrizione: DL-Glyceric acid 20% ∼2 mol/L in water

Fornitore: Thermo Scientific
Descrizione: Calcium-DL-glycerate hydrate

Bürkle single-use powder and liquid funnels

Cleanroom manufactured funnels, a practical and hygienic pouring aid! Also available sterile (10-6). Made of PS, compliant to EU food and FDA regulations.

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A truly clean filling aid for your lab

Codice catalogo: (TCIAG0232-10G)
Fornitore: TCI EUROPE
Codice articolo fornitore: G0232-10G
Codice articolo locale: TCIAG0232-10G
Descrizione: Calcium-DL-glycerate hydrate ≥98.0% (by titrimetric analysis)
UOM: 1 * 10 g


Codice catalogo: (BOSSBS-13448R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-CY3
Codice articolo locale: BOSSBS-13448R-CY3
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-A555
Codice articolo locale: BOSSBS-13448R-A555
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-CY5
Codice articolo locale: BOSSBS-13448R-CY5
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-FITC
Codice articolo locale: BOSSBS-13448R-FITC
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-A680
Codice articolo locale: BOSSBS-13448R-A680
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-A647
Codice articolo locale: BOSSBS-13448R-A647
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-HRP
Codice articolo locale: BOSSBS-13448R-HRP
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-CY7
Codice articolo locale: BOSSBS-13448R-CY7
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Fornitore: TCI EUROPE
Descrizione: Methyl (R)-(+)-2,2-dimethyl-1,3-dioxolane-4-carboxylate ≥98.0% (by GC)

Codice catalogo: (BOSSBS-13448R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-A488
Codice articolo locale: BOSSBS-13448R-A488
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-A750
Codice articolo locale: BOSSBS-13448R-A750
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. localised to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyse the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterised by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-13448R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-13448R-A350
Codice articolo locale: BOSSBS-13448R-A350
Descrizione: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.
UOM: 1 * 100 µl


Fornitore: Apollo Scientific
Descrizione: Methyl (R)-(+)-2,2-dimethyl-1,3-dioxolane-4-carboxylate

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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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