4-Chloro-1,6-naphthyridine
Artikel-Nr:
(91265.180)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC91265.180
Beschreibung:
16 components: Ag 10 mg/l, Al 100 mg/l, As 100 mg/l, Ba 50 mg/l, Be 5 mg/l, Cd 5 mg/l, Co 50 mg/l, Cr 20 mg/l, Cu 50 mg/l, Fe 20 mg/l, Mn 20 mg/l, Ni 50 mg/l, Pb 100 mg/l, Sb 100 mg/l, Se 100 mg/l, Tl 100 mg/l in 5% HNO₃
VE:
1 * 100 mL
Lieferant:
SGE Analytical Science
Beschreibung:
These reusable ferrules are made from 100% graphite. They have a temperature limit of 450 °C.
Artikel-Nr:
(BOSSBS-11130R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R
Lokale Artikelnummer::
BOSSBS-11130R
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-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R-CY5
Lokale Artikelnummer::
BOSSBS-11130R-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 KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
VE:
1 * 100 µl
Lieferant:
SGE Analytical Science
Beschreibung:
Needle, Gauge: 16, Länge: 70 mm, Ø ext.: 1,57 mm, Spitzentyp: abgeschrägt, NLL-7/16
Artikel-Nr:
(BOSSBS-9023R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R
Lokale Artikelnummer::
BOSSBS-9023R
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. alternatively splicing events.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Miltefosine
Artikel-Nr:
(BOSSBS-9629R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9629R-A750
Lokale Artikelnummer::
BOSSBS-9629R-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 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.
VE:
1 * 100 µl
Lieferant:
VWR Collection
Beschreibung:
PS. Diese Schalen für mikrobiologische Anwendungen werden unter strengen aseptischen Bedingungen hergestellt und verpackt (ISO 6).
Artikel-Nr:
(BOSSBS-9023R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R-A647
Lokale Artikelnummer::
BOSSBS-9023R-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. alternatively splicing events.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Curcumin 97%
Lieferant:
GLASWARENFABRIK KARL HECHT
Beschreibung:
Kalk-Natron-Glas.
Artikel-Nr:
(558-0190)
Lieferant:
SGE Analytical Science
Hersteller-Artikelnummer::
072650
Lokale Artikelnummer::
SGEA072650
Beschreibung:
The capillary cutting tool is used for burr free cutting of fused silica tubing.
VE:
1 * 20 ST
Lieferant:
VWR Collection
Beschreibung:
Mit rundem oder konischem Boden, mit oder ohne Graduierungen verfügbar. Nicht zur Verwendung unter starker Hitze und raschen Temperaturänderungen geeignet.
Artikel-Nr:
(BOSSBS-11130R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R-A488
Lokale Artikelnummer::
BOSSBS-11130R-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 KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11130R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R-HRP
Lokale Artikelnummer::
BOSSBS-11130R-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 KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
VE:
1 * 100 µl
Preis auf Anfrage
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