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1,6-Anhydro-\\u03B2-D-mannopyranose
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1,6-Anhydro-\\u03B2-D-mannopyranose
Artikel-Nr:
(BOSSBS-12225R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12225R-HRP
Lokale Artikelnummer::
BOSSBS-12225R-HRP
Beschreibung:
ZNF843 is a 348 amino acid protein that is encoded by a gene which maps to 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 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 ZNF843 gene product has been provisionally designated MGC46336 pending further characterization.
VE:
1 * 100 µl
Lieferant:
HERAEUS
Beschreibung:
Trommelrotor für 8 Racks, 80x2 ml, 16 438×g, Für: Biofuge® Stratos
Artikel-Nr:
(APOSOR9557-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR9557-5G
Lokale Artikelnummer::
APOSOR9557-5G
Beschreibung:
Methyl-6-hydroxynicotinat 98%
VE:
1 * 5 g
Lieferant:
Avantor Fluid Handling
Beschreibung:
No more eye strain - front shield magnifies scale 16 percent for easier readings.
Lieferant:
Bohlender
Beschreibung:
PTFE.
Lieferant:
Bohlender
Beschreibung:
PTFE, white.
Lieferant:
Avantor Fluid Handling
Beschreibung:
Erzielen Sie mit einer intuitiven Touchscreen-Oberfläche einen hochpräzisen Mehrkanalfluss.
Artikel-Nr:
(535-0031)
Lieferant:
LABCONCO
Hersteller-Artikelnummer::
7522900
Lokale Artikelnummer::
LBCP7522900
Beschreibung:
Zubehör für Gefriertrockner, Trockenkammer mit 16 Anschlüssen, Edelstahl, 330×330 mm, für Freezone® 6, 12 und 18
VE:
1 * 1 ST
Lieferant:
Avantor Fluid Handling
Beschreibung:
Vielseitige Pumpe für Prozessanwendungen - mit intuitiver Touchscreen-Bedienoberfläch und verbesserter Verbindung.
Lieferant:
Sartorius Balances
Beschreibung:
Die Gewichte bestehen aus poliertem Messing.
Lieferant:
Merck
Beschreibung:
1-(Dimethylamino)-2-propanol zur Synthese, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-9629R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9629R-CY7
Lokale Artikelnummer::
BOSSBS-9629R-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.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9629R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9629R-CY5
Lokale Artikelnummer::
BOSSBS-9629R-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.
VE:
1 * 100 µl
Artikel-Nr:
(SGEA082780)
Lieferant:
SGE Analytical Science
Hersteller-Artikelnummer::
082780
Lokale Artikelnummer::
SGEA082780
Beschreibung:
Cutter for steel tubing.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-13197R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-A680
Lokale Artikelnummer::
BOSSBS-13197R-A680
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-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-FITC
Lokale Artikelnummer::
BOSSBS-13197R-FITC
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
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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