Esta buscando: alpha-D-Galactose-1-phosphate+dipotassium+salt+pentahydrate


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Proveedor: VWR Chemicals
Descripción: , anhidro ≥98% ACS

FDS

Proveedor: Avantor
Descripción: ≥98.0% (base secada) FCC, J.T.Baker®
Proveedor: TCI
Descripción: L-Thyroxine sodium salt pentahydrate ≥98.0% (by titrimetric analysis)

Proveedor: Avantor
Descripción: 98.0-100.5% (base secada) USP, J.T.Baker®

Proveedor: Thermo Fisher Scientific
Descripción: di-Potasio hidrogenofosfato ≥98.0% ACS
Proveedor: VWR Chemicals
Descripción: di-Potasio hidrogenofosfato trihidrato ≥99.0%, AnalaR NORMAPUR® para análisis
Proveedor: Thermo Fisher Scientific
Descripción: Appearance: White to yellow Powder

FDS

Proveedor: Thermo Fisher Scientific
Descripción: 1.0 M in water

FDS

Numero del catalogo: (BOSSBS-13267R-CY5)
Proveedor: Bioss
Descripción: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
UOM: 1 * 100 µl


Numero del catalogo: (A1042.1000)
Proveedor: PanReac AppliChem
Descripción: di-Potasio hidrogenofosfato
UOM: 1 * 1 kg


Proveedor: Thermo Fisher Scientific
Descripción: di-Potasio hidrogenofosfato trihidrato, grado reactivo
Proveedor: Thermo Fisher Scientific
Descripción: di-Potasio hidrogenofosfato trihidrato, extra puro

FDS

Numero del catalogo: (BOSSBS-13267R-CY3)
Proveedor: Bioss
Descripción: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
UOM: 1 * 100 µl


Numero del catalogo: (BOSSBS-13267R-HRP)
Proveedor: Bioss
Descripción: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
UOM: 1 * 100 µl


Proveedor: Thermo Fisher Scientific
Descripción: di-Potasio hidrogenofosfato, anhidro 99+% para análisis

FDS

Numero del catalogo: (BOSSBS-13267R-A750)
Proveedor: Bioss
Descripción: GALK2 is important in the first step of the galactose metabolism pathway. GALK1, which belongs to the GHMP kinase family of proteins, is a crucial enzyme for galactose metabolism, specifically converting ?d-galactose to galactose 1-phosphate. Defects in the gene encoding GALK1 can cause galactosemia II, an autosomal recessive disorder characterized by congenital cataracts during infancy, often within the first two weeks of life. In the adult population, galactosemia II can cause presenile cataracts that are secondary to accumulation of galactitol in the lens of the eye. A second gene, GALK2, encodes an enzyme with greater activity against GalNAc than galactose. GALK2 has been implicated in the salvage pathway for the reutilization of free GalNAc derived from the degradation of complex carbohydrates.
UOM: 1 * 100 µl


Consulta de precio
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
El stock para este material es limitada pero puede estar disponible en un almacén cerca de usted. Por favor, asegúrese de que ha iniciado sesión en la web para que el stock disponible se puede mostrar. Si el call sigue apareciendo y usted necesita ayuda, por favor llámenos al 902 222 897 o por email en webshop.es@avantorsciences.com.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta. Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto se trata de un artículo regulado sometido a normativa que restringe su venta.
Si procede, nos pondremos en contacto con usted para solicitarle la licencia o declaración de uso necesaria para poder proceder al suministro del producto.
Este producto ha sido bloqueado por su organización. Por favor, pónganse en contacto con su departamento de compras para obtener más información.
El producto original ya no está disponible. Su sustituto se muestra a continuación.
El producto(s) marcados con este símbolo están descatalogados - se venden hasta acabar stock. Pueden encontrar alternativas buscando con el número de catálogo VWR listado arriba. Si necesita más ayuda, por favor llame al Servicio de atención al cliente de VWR al 902.222.897.
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