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Product Image-ACRO410980025

Glicerina 99.6% ACS

Proveedor: Thermo Fisher Scientific
Descripción: Glicerina 99.6% ACS

FDS Certificados Environmentally Preferable

Image Unavailable-BOSSBS-12039R-A350

Anti-GDE1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Numero del catalogo: (BOSSBS-12039R-A350)
Proveedor: Bioss
Descripción: GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12039R-FITC

Anti-GDE1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Numero del catalogo: (BOSSBS-12039R-FITC)
Proveedor: Bioss
Descripción: GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM: 1 * 100 µl
Image Unavailable-J62819.14

Trimyristin 95%

Numero del catalogo: (J62819.14)
Proveedor: Thermo Fisher Scientific
Descripción: Trimyristin 95%
UOM: 1 * 25 g

FDS Certificados


Image Unavailable-J62419.14

Triolein ≥75%, tech.

Proveedor: Thermo Fisher Scientific
Descripción: Triolein ≥75%, tech.

FDS Certificados

Image Unavailable-EHERTRC-G601603-1G

α-Glicerofosfato de disodio hidrato (Mezcla de isómeros)

Numero del catalogo: (EHERTRC-G601603-1G)
Proveedor: EHRENSTORFER
Descripción: α-Glicerofosfato de disodio hidrato (Mezcla de isómeros)
UOM: 1 * 1 g

New Product


Image Unavailable-1.03000.9025

Triacetina 98.5-100.5% (by alkalimetry), EMPROVE® ESSENTIAL Ph. Eur., BP, USP, SAFC®

Proveedor: MERCK PRODUCTION CHEMICALS
Descripción: Triacetina 98.5-100.5% (by alkalimetry), EMPROVE® ESSENTIAL USP, Ph. Eur., BP suitable for use as excipient, SAFC®

FDS Certificados

Product Image-ACRO158920025

Glicerina 99+%, extra puro

Proveedor: Thermo Fisher Scientific
Descripción: Glicerina 99+%, extra puro

FDS

Product Image-ACRO332030025

Glicerina (sintético) 99+%, puro

Proveedor: Thermo Fisher Scientific
Descripción: Glicerina (sintético) 99+%, puro

FDS

Product Image-ACRO327255000

Glicerina 99.5% para biología molecular

Numero del catalogo: (ACRO327255000)
Proveedor: Thermo Fisher Scientific
Descripción: Glicerina 99.5% para biología molecular
UOM: 1 * 500 mL

FDS


Image Unavailable-EHERC14036500

Glicerina

Numero del catalogo: (EHERC14036500)
Proveedor: EHRENSTORFER
Descripción: Glicerina
UOM: 1 * 1 mL
Image Unavailable-BOSSBS-12039R-CY7

Anti-GDE1 Rabbit Polyclonal Antibody (Cy7®)

Numero del catalogo: (BOSSBS-12039R-CY7)
Proveedor: Bioss
Descripción: GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12039R-HRP

Anti-GDE1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Numero del catalogo: (BOSSBS-12039R-HRP)
Proveedor: Bioss
Descripción: GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM: 1 * 100 µl
Image Unavailable-ICNA0210529705

Tricaprin, white solid

Proveedor: MP Biomedicals
Descripción: Soluble in chloroform (100 mg/ml) and ethanol.

FDS

Image Unavailable-356350-1000

Glicerina, Millipore®

Proveedor: Merck Millipore (Calbiochem‎)
Descripción: Glicerina, Millipore®

Image Unavailable-ICNA0215119490

Glicerina, líquido

Proveedor: MP Biomedicals
Descripción: Glicerina, líquido

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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