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Image Unavailable-12609.22

Potasio carbonato ≥99.0% ACS

Proveedor: Thermo Fisher Scientific
Descripción: Potasio carbonato ≥99.0% ACS

FDS Certificados

Image Unavailable-BOSSBS-7593R-A350

Anti-GLA Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numero del catalogo: (BOSSBS-7593R-A350)
Proveedor: Bioss
Descripción: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Product Image-P0350-N5L

Cell culture media, Liebovitz L-15 medium

Proveedor: Biowest
Descripción: The Leibovitz L-15 media were formulated to promote the cell growth in medium not balanced in CO₂. The formulations were developed with the sodium bicarbonate buffer. The Leibovitz L-15 media are buffered by a complement of salts, free base amino acids and galactose so they can be used under conditions of free gaseous exchange with the atmosphere. When properly supplemented, L-15 Medium supports established cell lines, such as HEp-2 and LLC-MK2, as well as primary explants of embryonic and adult human tissue. Many viruses also have been successfully cultivated in this medium.

FDS Certificados

Image Unavailable-BOSSBS-13268R-CY5

Anti-GALM Rabbit Polyclonal Antibody (Cy5®)

Numero del catalogo: (BOSSBS-13268R-CY5)
Proveedor: Bioss
Descripción: Galactose Mutarotase is a member of the aldose epimerase family and is involved in hexose metabolism. Through its catalytic activity, Galactose Mutarotase converts beta-aldose to alpha-aldose on several sugars, including D-glucose, L-arabinose and D-xylose. Found in the cytoplasm of most cells, Galactose Mutarotase plays a key role in galactose metabolism by catalyzing the conversion of beta-D-galactose to alpha-D-galactose. The enzyme contains two residues, Glu 304 and His 170, that are critical for catalysis, as well as His 96 and Asp 243, which are important for proper substrate recognition by the active site. No known diseases have been associated with mutations in the Galactose Mutarotase gene, although inhibition of Galactose Mutarotase activity could potentially be associated with a build-up of unmetabolized sugars during metabolism.
UOM: 1 * 100 µl
Image Unavailable-PRLSMC310249.9010

Potasio carbonato

Numero del catalogo: (PRLSMC310249.9010)
Proveedor: PROLABO CMP
Descripción: Potasio carbonato
UOM: 1 * 10 L
Product Image-198040010.

Potasio carbonato, anhidro 99+% para análisis

Proveedor: Thermo Fisher Scientific
Descripción: Potasio carbonato, anhidro 99+% para análisis

FDS

Product Image-ACRO115240250

1,2:3,4-Di-O-isopropylidene-ɑ-D-galactopyranose 97%

Proveedor: Thermo Fisher Scientific
Descripción: Appearance: Clear colorless to yellow Viscous liquid or paste

FDS

Image Unavailable-10838.14

Potasio carbonato ≥99.997% (metals basis), Puratronic®

Proveedor: Thermo Fisher Scientific
Descripción: Potasio carbonato ≥99.997% (metals basis), Puratronic®

FDS Certificados

Image Unavailable-BOSSBS-7593R-FITC

Anti-GLA Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numero del catalogo: (BOSSBS-7593R-FITC)
Proveedor: Bioss
Descripción: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-TCIAD2555-5G

1,2:3,4-Di-O-isopropylidene-ɑ-D-galactopyranose ≥92.0% (por GC)

Proveedor: TCI
Descripción: 1,2:3,4-Di-O-isopropylidene-ɑ-D-galactopyranose ≥92.0% (por GC)

Image Unavailable-BOSSBS-7593R-CY5.5

Anti-GLA Rabbit Polyclonal Antibody (Cy5.5®)

Numero del catalogo: (BOSSBS-7593R-CY5.5)
Proveedor: Bioss
Descripción: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-CY7

Anti-GLA Rabbit Polyclonal Antibody (Cy7®)

Numero del catalogo: (BOSSBS-7593R-CY7)
Proveedor: Bioss
Descripción: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Product Image-ACRO434920050

N-Acetyl-D-galactosamine 98%

Proveedor: Thermo Fisher Scientific
Descripción: N-Acetyl-D-galactosamine 98%

FDS

Image Unavailable-BOSSBS-7593R-HRP

Anti-GLA Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numero del catalogo: (BOSSBS-7593R-HRP)
Proveedor: Bioss
Descripción: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-7593R-A647

Anti-GLA Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Numero del catalogo: (BOSSBS-7593R-A647)
Proveedor: Bioss
Descripción: Galactosidase alpha is involved in the hydrolysis of terminal, non reducing alpha D galactose residues in alpha D galactosides, including galactose oligosaccharides, galactomannans and galactohydrolase. Defects in GLA are the cause of Fabry's disease (FD). FD is a rare X-linked sphingolipidosis disease where glycolipid accumulates in many tissues. Clinical recognition in males results from characteristic skin lesions (angiokeratomas) over the lower trunk. Patients may show ocular deposits, febrile episodes, and burning pain in the extremities. Death results from renal failure, cardiac or cerebral complications of hypertension or other vascular disease. Heterozygous females may exhibit the disorder in an attenuated form, they are more likely to show corneal opacities.
UOM: 1 * 100 µl
Image Unavailable-APOSIN2896-25G

Potasio carbonato 99.99%

Numero del catalogo: (APOSIN2896-25G)
Proveedor: Apollo Scientific
Descripción: Potasio carbonato 99.99%
UOM: 1 * 25 g
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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