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DIAGNOSTIC+SYSTEMS+DIASYS
Artikel-Nr:
(BOSSBS-12548R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12548R-A647
Lokale Artikelnummer::
BOSSBS-12548R-A647
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5789R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5789R-A680
Lokale Artikelnummer::
BOSSBS-5789R-A680
Beschreibung:
Zn(2+) acts as a agonist. This receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. Its effect is mediated mainly through G(q)-alpha and G(12)/G(13) proteins. Involved in regulation of body weight, gastrointestinal mobility, hormone secretion and cell death (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7698R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7698R-A680
Lokale Artikelnummer::
BOSSBS-7698R-A680
Beschreibung:
The protein encoded by this gene is a member of the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein might play a role in neurogenesis in the central nervous system. Two transcript variants encoding different isoforms have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11071R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11071R-A750
Lokale Artikelnummer::
BOSSBS-11071R-A750
Beschreibung:
This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11130R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R-FITC
Lokale Artikelnummer::
BOSSBS-11130R-FITC
Beschreibung:
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 KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11130R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R-A555
Lokale Artikelnummer::
BOSSBS-11130R-A555
Beschreibung:
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 KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9729R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R-A680
Lokale Artikelnummer::
BOSSBS-9729R-A680
Beschreibung:
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 characterised 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 tumour 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 characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7341R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-A647
Lokale Artikelnummer::
BOSSBS-7341R-A647
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9915R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9915R-A750
Lokale Artikelnummer::
BOSSBS-9915R-A750
Beschreibung:
Orosomucoid 2 is a key acute phase plasma protein. Because of its increase due to acute inflammation, this protein is classified as an acute-phase reactant. The specific function of this protein has not yet been determined; however Orosomucoid 2 appears to function in modulating the activity of the immune system during the acute-phase reaction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6092R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6092R-CY5
Lokale Artikelnummer::
BOSSBS-6092R-CY5
Beschreibung:
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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6349R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6349R-CY5
Lokale Artikelnummer::
BOSSBS-6349R-CY5
Beschreibung:
May be involved in the regulation of cell-cell interactions or in synatogenesis during the maturation of the nervous system. NERP peptides are involved in the control of body fluid homeostasis by regulating vasopressin release. Antimicrobial peptide VGF[554-577]: Has bactericidal activity against M. luteus, and antifungal activity against P. Pastoris.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6349R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6349R-CY5.5
Lokale Artikelnummer::
BOSSBS-6349R-CY5.5
Beschreibung:
May be involved in the regulation of cell-cell interactions or in synatogenesis during the maturation of the nervous system. NERP peptides are involved in the control of body fluid homeostasis by regulating vasopressin release. Antimicrobial peptide VGF[554-577]: Has bactericidal activity against M. luteus, and antifungal activity against P. Pastoris.
VE:
1 * 100 µl
Lieferant:
VWR Collection
Beschreibung:
Eine Auswahl an binokularen und trinokularen Stereo-Zoom-Mikroskopköpfen für grundlegende oder fortgeschrittenere Anforderungen.
Lieferant:
LABCONCO
Beschreibung:
XPert™ balance enclosures provide user protection by keeping powders, particulates and fume contained during weighing procedures. They are well suited for pharmaceutical research and other laboratory applications involving weighing of toxic substances. These vented balance safety enclosures may be ducted to the outside or connected to the FilterMate Portable Exhauster to be exhausted back into the laboratory through HEPA filters.
Artikel-Nr:
(BOSSBS-3635R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3635R-CY5
Lokale Artikelnummer::
BOSSBS-3635R-CY5
Beschreibung:
The H3 subclass of histamine receptors could mediate the histamine signals in CNS and peripheral nervous system. Signals through the inhibition of adenylate cyclase and displays high constitutive activity (spontaneous activity in the absence of agonist). Agonist stimulation of isoform 3 neither modified adenylate cyclase activity nor induced intracellular calcium mobilization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11556R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11556R-CY7
Lokale Artikelnummer::
BOSSBS-11556R-CY7
Beschreibung:
FOXB1 and FOXB2 are winged helix/forkhead transcription factors. FOXB1 is specifically expressed in the developing central nervous system (CNS). Early embryonic FOXB1 expression is restricted to the mammiliary body region of the caudal hypothalamus, midbrain, hindbrain and spinal cord. FOXB1 may play a role in postnatal growth, lactation and CNS development.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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