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Masterflex®+L/S®+MasterSense™+Fill/Finish+Pump+System
Numéro de catalogue:
(BOSSBS-9729R-CY3)
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-12548R-CY3)
Fournisseur:
Bioss
Description:
Subunit of the integral membrane V0 complex of vacuolar ATPase. Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells, thus providing most of the energy required for transport processes in the vacuolar system. May play a role in coupling of proton transport and ATP hydrolysis (By similarity).
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15088R-FITC)
Fournisseur:
Bioss
Description:
C1s B chain is a serine protease that combines with C1q and C1r to form C1, the first component of the classical pathway of the complement system. C1r activates C1s so that it can, in turn, activate C2 and C4.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15088R-A750)
Fournisseur:
Bioss
Description:
C1s B chain is a serine protease that combines with C1q and C1r to form C1, the first component of the classical pathway of the complement system. C1r activates C1s so that it can, in turn, activate C2 and C4.
UOM:
1 * 100 µl
Numéro de catalogue:
(PB009C-1-DM2)
Fournisseur:
Charles River Laboratories Cell Solutions
Description:
Mononuclear cells used for researching the causes, diagnosis, supportive care and treatment of Diabetes Mellitus 2 (DM2), the most common form of diabetes. Human mononuclear cells are collected from human volunteer donors diagnosed with DM2 under IRB approved informed consent by whole blood or leukapheresis using the COBE® Spectra Apheresis System MNC collection protocol.
UOM:
1 * 1 EA
Fournisseur:
Brady
Description:
Workstation print partner suite is a package of the Workstation print partner application and Advanced Import and Sequence extensions in a single bundle.
Numéro de catalogue:
(BOSSBS-1251R-HRP)
Fournisseur:
Bioss
Description:
Cell adhesion molecule that binds to CD6. Involved in neurite extension by neurons via heterophilic and homophilic interactions. May play a role in the binding of T- and B-cells to activated leukocytes, as well as in interactions between cells of the nervous system.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-6092R-CY5.5)
Fournisseur:
Bioss
Description:
RHOBTB1 is a member of the Rho family of the small GTPase superfamily. Is made of a GTPase domain, a proline-rich region, a tandem of 2 BTB (broad complex, tramtrack, and bric-a-brac) domains, and a conserved C-terminal region. Plays a role in small GTPase-mediated signal transduction and the organization of the actin filament system.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-12056R-A750)
Fournisseur:
Bioss
Description:
Serotonin (also designated 5-hydroxytryptamine or 5-HT) is a molecule that functions as a neurotransmitter, a hormone and a mitogen, and it is predominantly expressed in the gut, platelets and central nervous system (CNS). In the CNS, serotonin modulates several processes, including anxiety, sleep, appetite, behavior and drug abuse. In platelets and gut, serotonin plays a major role in cardiovascular function and motility of the gastrointestinal tract, respectively. Serotonin mediates its effects through several of G protein coupled receptors, designated 5-HT receptors or alternatively SR receptors. SR-3 is a ligand-gated ion channel, whereas all other known serotonin receptor subtypes are G protein-coupled receptors. SR-4 mediates widespread effects in central and peripheral nervous systems. SR-7 belongs to the superfamily of G protein-coupled receptors. The gene which encodes SR-7 maps to human chromosome 10q21-q24.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8411R-A350)
Fournisseur:
Bioss
Description:
Cysteine-rich secretory proteins (CRISPs) represent a family of evolutionarily conserved proteins that may play a role in the innate immune system and are transcriptionally regulated by androgens in several tissues. GAPR-1 (Golgi-associated plant pathogenesis-related protein 1), also known as GLIPR2, is a 154 amino acid lipid anchor protein belonging to the CRISP family. GAPR-1 also shares similarity with the pathogenesis-related protein (PR) superfamily, and may play an important role in the immune system. Existing as a homodimer, GAPR-1 is highly expressed in lung and peripheral leukocytes with minor expression in liver and kidney. Containing a conserved sperm-coating protein (SCP) domain, GAPR-1 binds to negatively charged lipids and may be involved in the differentiation of epithelial cells into mesenchymal cells. Increased expression of GAPR-1 in kidney may contribute to the development of fibrosis.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9632R-FITC)
Fournisseur:
Bioss
Description:
PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.
UOM:
1 * 100 µl
Fournisseur:
Biotium
Description:
The Lewis histo-blood group system comprises a set of fucosylated glycosphingolipids that are synthesized by exocrine epithelial cells and circulate in body fluids. The glycosphingolipids function in embryogenesis, tissue differentiation, tumor metastasis, inflammation, and bacterial adhesion. They are secondarily absorbed to red blood cells giving rise to their Lewis phenotype. This gene is a member of the fucosyltransferase family, which catalyzes the addition of fucose to precursor polysaccharides in the last step of Lewis antigen biosynthesis. It encodes an enzyme with alpha(1,3)-fucosyltransferase and alpha(1,4)-fucosyltransferase activities. Lewis blood group antigens are carbohydrate moieties structurally integrated in mucous secretions. Lewis antigen system alterations have been described in gastric carcinoma and associated lesions. Anomalous expression of Lewis B antigen has been found in some non-secretory gastric carcinomas and colorectal cancers.
Numéro de catalogue:
(BOSSBS-15464R-A350)
Fournisseur:
Bioss
Description:
HERPUD1 is a includes the inhibition of translation to prevent further accumulation of unfolded proteins, the increased expression of proteins involved in polypeptide folding, known as the unfolded protein response (UPR), and the destruction of misfolded proteins by the ER-associated protein degradation (ERAD) system. This gene may play a role in both UPR and ERAD. Its expression is induced by UPR and it has an ER stress response element in its promoter region while the encoded protein has an N-terminal ubiquitin-like domain which may interact with the ERAD system. This protein has been shown to interact with presenilin proteins and to increase the level of amyloid-beta protein following its overexpression. Alternative splicing of this gene produces multiple transcript variants encoding different isoforms. The full-length nature of all transcript variants has not been determined.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15464R-A680)
Fournisseur:
Bioss
Description:
HERPUD1 is a includes the inhibition of translation to prevent further accumulation of unfolded proteins, the increased expression of proteins involved in polypeptide folding, known as the unfolded protein response (UPR), and the destruction of misfolded proteins by the ER-associated protein degradation (ERAD) system. This gene may play a role in both UPR and ERAD. Its expression is induced by UPR and it has an ER stress response element in its promoter region while the encoded protein has an N-terminal ubiquitin-like domain which may interact with the ERAD system. This protein has been shown to interact with presenilin proteins and to increase the level of amyloid-beta protein following its overexpression. Alternative splicing of this gene produces multiple transcript variants encoding different isoforms. The full-length nature of all transcript variants has not been determined.
UOM:
1 * 100 µl
Fournisseur:
G-Biosciences
Description:
OptiBlaze™ ELISA femto-HRP and femto-AP are stabilised ultra sensitive luminol and 1,2 dioxetane based horseradish peroxidase or alkaline phosphatase substrates for the detection of HRP or AP-conjugated antibodies during ELISA.
Numéro de catalogue:
(D1086-02)
Fournisseur:
OMEGA BIO-TEK
Description:
Le kit E-Z 96® Plant DNA permet l'isolation rapide et fiable de l'ADN cellulaire total de haute qualité à partir d'un grand nombre d'espèces de plantes et de tissus dans un format 96 puits. Les kits E-Z 96® Plant DNA utilisent un système de tampon adapté à partir du système SP Plant DNA, qui convient pour de nombreuses plantes, telles que celles dont le niveau de composés phénoliques ou de polysaccharides est anormalement élevé (par exemple, les échantillons de coton, de pin et d'arachide). Il est possible de traiter jusqu'à 50 mg de tissu humide ou 12 mg de tissu sec dans chaque puits, en moins d'une heure. Afin d'éliminer les polysaccharides, composés phénoliques et inhibiteurs d'enzyme des lysats de tissus de plantes, ce système associe les propriétés de liaisons d'acide nucléique réversibles de la matrice HiBind avec la vitesse et la polyvalence de la plaque E-Z 96® DNA. L'ADN purifié convient pour PCR, digestion par des enzymes de restriction et techniques d'hybridation.
UOM:
1 * 1 KIT
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