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1,6-Dibromo-2,5-dioxaperfluorohexane
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1,6-Dibromo-2,5-dioxaperfluorohexane
Lieferant:
Avantor Fluid Handling
Beschreibung:
Kein Aufquellen oder Verspröden.
Artikel-Nr:
(BOSSBS-7341R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-CY5
Lokale Artikelnummer::
BOSSBS-7341R-CY5
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
Lieferant:
Thermo Scientific
Beschreibung:
3,3-Dimethylbutyraldehyd
Artikel-Nr:
(BOSSBS-7341R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-CY3
Lokale Artikelnummer::
BOSSBS-7341R-CY3
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-7341R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R
Lokale Artikelnummer::
BOSSBS-7341R
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:
(521-4197)
Lieferant:
BECKMAN COULTER
Hersteller-Artikelnummer::
B88554
Lokale Artikelnummer::
BECMB88554
Beschreibung:
JA-14.50 fixed angle (high performance) aluminium rotor, with BioSafe dual-locking lid, 16×50 ml conical, 14000 rpm, 35000×g for use in Avanti J Series centrifuges
VE:
1 * 1 ST
Lieferant:
ENTEGRIS
Beschreibung:
These tube fittings are made from PFA.
Artikel-Nr:
(548-0496A)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI548-0496A
Beschreibung:
Rollrand-ND13-Fläschchen aus Borosilikatglas der 1. hydrolytischen Klasse mit flachem Boden. Sie sind mit einer Vielzahl von Aluminiumsiegeln und Septenmaterialien erhältlich.
VE:
1 * 1.000 ST
Artikel-Nr:
(B20395.03)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
B20395.03
Lokale Artikelnummer::
ALFAB20395.03
Beschreibung:
2,4,5-Trifluorphenol ≥94%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-7341R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-A750
Lokale Artikelnummer::
BOSSBS-7341R-A750
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 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 characterisation.
VE:
1 * 100 µl
Lieferant:
Bohlender
Beschreibung:
Silikon mit PTFE-Stulpe
Artikel-Nr:
(BOSSBS-9729R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R-CY7
Lokale Artikelnummer::
BOSSBS-9729R-CY7
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:
(8.14784.0100)
Lieferant:
Merck
Hersteller-Artikelnummer::
8.14784.0100
Lokale Artikelnummer::
MERC8.14784.0100
Beschreibung:
Trifluoroborane acetonitrile complex, Sigma-Aldrich®
VE:
1 * 100 mL
Artikel-Nr:
(BOSSBS-7341R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-HRP
Lokale Artikelnummer::
BOSSBS-7341R-HRP
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
Lieferant:
KEYSTONE CLEANROOM PRODUCTS
Beschreibung:
Sparen Sie Zeit und standardisieren Sie die Aktivitäten zum Vorbereiten der Ausrüstung für Sterilisationen.
Preis auf Anfrage
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.
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
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