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4-Chloro-1,6-naphthyridine
Artikel-Nr:
(ABCAAB207181-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB207181-100
Lokale Artikelnummer::
ABCAAB207181-100
Beschreibung:
Anti-IL-16 Rabbit Monoclonal Antibody [clone: EPR19988]
VE:
1 * 100 µl
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-13197R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-A647
Lokale Artikelnummer::
BOSSBS-13197R-A647
Beschreibung:
C16orf63, also known as FLJ31153 or DKFZp686N1651, is a 174 amino acid protein that contains one LisH domain. The gene that encodes C16orf63 maps to human chromosome 16. 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 C16orf63 gene product has been provisionally designated C16orf63 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13197R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-HRP
Lokale Artikelnummer::
BOSSBS-13197R-HRP
Beschreibung:
C16orf63, also known as FLJ31153 or DKFZp686N1651, is a 174 amino acid protein that contains one LisH domain. The gene that encodes C16orf63 maps to human chromosome 16. 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 C16orf63 gene product has been provisionally designated C16orf63 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13197R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-A350
Lokale Artikelnummer::
BOSSBS-13197R-A350
Beschreibung:
C16orf63, also known as FLJ31153 or DKFZp686N1651, is a 174 amino acid protein that contains one LisH domain. The gene that encodes C16orf63 maps to human chromosome 16. 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 C16orf63 gene product has been provisionally designated C16orf63 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13197R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-A750
Lokale Artikelnummer::
BOSSBS-13197R-A750
Beschreibung:
C16orf63, also known as FLJ31153 or DKFZp686N1651, is a 174 amino acid protein that contains one LisH domain. The gene that encodes C16orf63 maps to human chromosome 16. 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 C16orf63 gene product has been provisionally designated C16orf63 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR946325-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR946325-1G
Lokale Artikelnummer::
APOSOR946325-1G
Beschreibung:
5-(1-Hydroxyethyl)-2-methylpyridine 95%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Ethynyltetrahydropyran-4-ol 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Inhibits glucose transport.
Lieferant:
Alfa Aesar
Beschreibung:
Maleinsäure ≥98%
Lieferant:
Alfa Aesar
Beschreibung:
α,α-Dimethylpropiophenon ≥98%
Lieferant:
Alfa Aesar
Beschreibung:
2-Ethylfuran ≥98%
Artikel-Nr:
(BURK5620-2181)
Lieferant:
BURKLE
Hersteller-Artikelnummer::
5620-2181
Lokale Artikelnummer::
BURK5620-2181
Beschreibung:
The vacuum hand pump can be operated with one hand to create a vacuum or pressure, independent of power supply.
VE:
1 * 1 ST
Artikel-Nr:
(734-0678)
Lieferant:
Spectrum Laboratories
Hersteller-Artikelnummer::
132700
Lokale Artikelnummer::
SPEC132700
Beschreibung:
MWCO 12 - 14 kD, regenerierte Cellulose.
VE:
1 * 30 m
Artikel-Nr:
(BOSSBS-9629R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9629R-CY3
Lokale Artikelnummer::
BOSSBS-9629R-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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9629R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9629R
Lokale Artikelnummer::
BOSSBS-9629R
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.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Isothiazole 97%
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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