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5-Chloro-1,6-naphthyridine
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5-Chloro-1,6-naphthyridine
Artikel-Nr:
(APOSOR470655-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR470655-1G
Lokale Artikelnummer::
APOSOR470655-1G
Beschreibung:
3-Ethoxypyridin-2(1H)-one
VE:
1 * 1 g
Lieferant:
Simport Scientific
Beschreibung:
Die idealen Verschlüsse für Reagenz-, Proben- und Kulturröhrchen aus Glas und Plastik, LDPE, farbig.
Lieferant:
Alfa Aesar
Beschreibung:
Ethyl-4,4,4-trifluorcrotonat ≥98%
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:
(LENZ01300018)
Lieferant:
Lenz Laborglas GmbH & CO.KG
Hersteller-Artikelnummer::
01300018
Lokale Artikelnummer::
LENZ01300018
Beschreibung:
DURAN®, Borosilikatglas, klar.
VE:
1 * 1 ST
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
Lieferant:
RSG
Beschreibung:
Doppelenden, schmale Spatel aus Edelstahl. In flexibel oder nicht flexibel verfügbar.
Lieferant:
Thermo Scientific
Beschreibung:
Isothiazole 97%
Lieferant:
ENTEGRIS
Beschreibung:
These tube fittings are made from PFA.
Artikel-Nr:
(734-0672)
Lieferant:
Spectrum Laboratories
Hersteller-Artikelnummer::
132678
Lokale Artikelnummer::
SPEC132678
Beschreibung:
MWCO 12 - 14 kD, regenerierte cellulose.
VE:
1 * 15 m
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Cyclopropylpyridin-3-amine
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Ethoxy-2-nitroaniline
Lieferant:
Advanced Chromatography Technologies
Beschreibung:
Diese Edelstahlsäulen mit proprietärer Verbindungstechnologie bieten hohe Robustheit bei ausgezeichneter Säulenlebensdauer.
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
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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