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1,8-Diazabicyclo[5.4.0]-7-undecen
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1,8-Diazabicyclo[5.4.0]-7-undecen
Artikel-Nr:
(BOSSBS-8405R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8405R-A350
Lokale Artikelnummer::
BOSSBS-8405R-A350
Beschreibung:
GFOD2 is a 385 amino acid secreted protein of the extracellular matrix that belongs to the gfo/idh/mocA family. Existing as two alternatively spliced isoforms, GFOD2 enhances matrix assembly and is encoded by a gene that maps to human chromosome 16q22.1. Chromosome 16 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.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
(+/-)-Sulpiride
Lieferant:
DWK Life Sciences
Beschreibung:
Kalk-Soda-Glas mit DIN-Gewinde und PP-Schraubverschlusskappe.
Artikel-Nr:
(BOSSBS-9037R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9037R-CY3
Lokale Artikelnummer::
BOSSBS-9037R-CY3
Beschreibung:
Proteins containing PDZ domains have been shown frequently to bind the C-termini of transmembrane receptors or ion channels. They have also been shown to bind to other PDZ domain proteins and could possibly be involved in intracellular signalling. PDZK3 contains six PDZ domains and shares sequence similarity with pro-interleukin-16 (pro-IL-16). Like pro-IL-16, the encoded protein localizes to the endoplasmic reticulum and is thought to be cleaved by a caspase to produce a secreted peptide containing two PDZ domains. In addition, the PDZK3 gene is upregulated in primary prostate tumors and may be involved in the early stages of prostate tumorigenesis.
VE:
1 * 100 µl
Lieferant:
ENTEGRIS
Beschreibung:
These tube fittings are made from PVDF, PFA or CPFA.
Lieferant:
VWR Chemicals
Beschreibung:
Die Zusammensetzung des Materials kann zwischen 16- und 18-Hydrat variieren.
Artikel-Nr:
(620-2277)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI620-2277
Beschreibung:
Dieses praktische Messgerät mit Dreifach-Anzeige misst kontinuierlich alle Parameter. Akustischer und visueller LED-Alarm kann bei drei verschiedenen Luftfeuchtigkeitswerten ausgelöst werden (55%, 60% oder 65%). Festkörpersensoren liefern schnelle Messergebnisse in weniger als 30 Sekunden.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-9729R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R-FITC
Lokale Artikelnummer::
BOSSBS-9729R-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 FAM96B gene product has been provisionally designated FAM96B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11130R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R-A350
Lokale Artikelnummer::
BOSSBS-11130R-A350
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-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R-A488
Lokale Artikelnummer::
BOSSBS-9729R-A488
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 FAM96B gene product has been provisionally designated FAM96B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9729R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R-A647
Lokale Artikelnummer::
BOSSBS-9729R-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 FAM96B gene product has been provisionally designated FAM96B pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR200156-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR200156-1G
Lokale Artikelnummer::
APOSOR200156-1G
Beschreibung:
2-(Methylsulphanyl)benzamide
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-P-Tolylpyridine-3-carbaldehyde 95%
Lieferant:
Lenz Laborglas GmbH & CO.KG
Beschreibung:
Silicone rubber sealing rings with PTFE washers.
Lieferant:
Advanced Chromatography Technologies
Beschreibung:
Diese ultra-inerten Avantor® ACE® C18-HL-Säulen bieten eine hervorragende Reproduzierbarkeit und Säulenlebensdauer. Diese kapillaren bis präparativen Edelstahlsäulen sind in einer Vielzahl von Partikelgrößen und -abmessungen erhältlich.
Artikel-Nr:
(BOSSBS-8320R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8320R-A647
Lokale Artikelnummer::
BOSSBS-8320R-A647
Beschreibung:
HEATR3 is a 680 amino acid protein existing as three alternatively spliced isoforms and containing two HEAT (Huntingtin, elongation factor 3 (EF3), protein phosphatase 2A (PP2A) and the yeast PI3-kinase Tor1) repeats. HEAT repeats form rod-like helical structures that are involved in intracellular transport. HEATR3 is encoded by a gene located on 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, a gastrointestinal inflammatory condition.
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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