Recherche de texte >
Masterflex®+L/S®+MasterSense™+Fill/Finish+Pump+System
Imprimer
Votre recherche pour:
50 149 les résultats ont été trouvés
Masterflex®+L/S®+MasterSense™+Fill/Finish+Pump+System
Numéro de catalogue:
(BOSSBS-11330R-CY3)
Fournisseur:
Bioss
Description:
There are three sorCS genes that have diverse, partially overlapping functions in the central nervous system. In the developing and mature central nervous system, the homologous SorCS1 and SorCS2 genes and the SorCS3 gene are expressed in a combinatorial, non-overlapping pattern. SorCS proteins show homology to the mosaic receptor SorLA and the neurotensin receptor sortilin, based on a common VPS10 domain, which is the hallmark of the SorCS receptor family. SorCS1 is a type 1 receptor containing a VPS10P domain and a leucine-rich domain. Alternative splicing of human SorCS1 results in four isoforms with different cytoplasmic tails and differential expression in tissues. Human SorCS1 is detected in fetal and infant brain and in fetal retina. Alternative splicing of murine SorCS1 also results in four isoforms. Murine isoform 1 is highly expressed in brain and at lower levels in heart, liver and kidney. It is detected in newborn mouse brain and in adult olfactory bulb and cerebral cortex. Murine isoform 2 is highly expressed in liver and at lower levels in heart, brain, kidney and testis.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-7341R-A350)
Fournisseur:
Bioss
Description:
Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The C16orf72 gene product has been provisionally designated C16orf72 pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9729R-A555)
Fournisseur:
Bioss
Description:
Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The FAM96B gene product has been provisionally designated FAM96B pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-11330R-HRP)
Fournisseur:
Bioss
Description:
There are three sorCS genes that have diverse, partially overlapping functions in the central nervous system. In the developing and mature central nervous system, the homologous SorCS1 and SorCS2 genes and the SorCS3 gene are expressed in a combinatorial, non-overlapping pattern. SorCS proteins show homology to the mosaic receptor SorLA and the neurotensin receptor sortilin, based on a common VPS10 domain, which is the hallmark of the SorCS receptor family. SorCS1 is a type 1 receptor containing a VPS10P domain and a leucine-rich domain. Alternative splicing of human SorCS1 results in four isoforms with different cytoplasmic tails and differential expression in tissues. Human SorCS1 is detected in fetal and infant brain and in fetal retina. Alternative splicing of murine SorCS1 also results in four isoforms. Murine isoform 1 is highly expressed in brain and at lower levels in heart, liver and kidney. It is detected in newborn mouse brain and in adult olfactory bulb and cerebral cortex. Murine isoform 2 is highly expressed in liver and at lower levels in heart, brain, kidney and testis.
UOM:
1 * 100 µl
Numéro de catalogue:
(AVIVARP49658_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-TMEM35 Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP38277_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-TEAD3 Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVAVARP13036P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-GAL Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVAVARP13038T100)
Fournisseur:
Aviva Systems Biology
Description:
Anti-GRIA2 Rabbit Polyclonal Antibody
UOM:
1 * 100 µl
Numéro de catalogue:
(AVIVARP50685_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-ZNF385D Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP50729_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-SARNP Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP57121_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-CENPQ Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP58401_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-CDK1 Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP57105_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-MAP7D1 Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP33947_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-KIF23 Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP34011_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-HNF1B Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(AVIVARP33967_P050)
Fournisseur:
Aviva Systems Biology
Description:
Anti-KIF9 Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Appel de prix
Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l'
 est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
Le stock de cet article est limité mais peut être disponible dans un entrepôt proche de vous. Merci de vous assurer que vous êtes connecté sur le site afin que le stock disponible soit affiché. Si l'
est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
Ces articles ne peuvent être ajoutés au Panier. Veuillez contacter votre service client ou envoyer un e-mail à vwr.be@vwr.com
Une documentation supplémentaire peut être nécessaire pour l'achat de cet article. Un représentant de VWR vous contactera si nécessaire.
Ce produit a été bloqué par votre organisation. Contacter votre service d'achat pour plus d'informations.
Le produit original n'est plus disponible. Le remplacement représenté est disponible
Les produits marqués de ce symbole ne seront bientôt plus disponibles - vente jusqu'à épuisement de stock. Des alternatives peuvent être disponibles en recherchant le code article VWR indiqué ci-dessus. Si vous avez besoin d'une assistance supplémentaire, veuillez contacter notre Service Clientèle au 016 385 011.
|
|||||||||
Vue liste
