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1,6-Anhydro-\\u03B2-D-mannopyranose
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1,6-Anhydro-\\u03B2-D-mannopyranose
Artikel-Nr:
(SCOR1028141)
Lieferant:
Schott AG
Hersteller-Artikelnummer::
1028141
Lokale Artikelnummer::
SCOR1028141
Beschreibung:
Made of AR®-Glas.
VE:
1 * 15,1 kg
Artikel-Nr:
(ACRO461830010)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
461830010
Lokale Artikelnummer::
ACRO461830010
Beschreibung:
Miltefosine 98%
VE:
1 * 1 g
Artikel-Nr:
(212-6258)
Lieferant:
Bel-Art Products, a Part of SP
Hersteller-Artikelnummer::
F188640001
Lokale Artikelnummer::
BELAF188640001
Beschreibung:
PP, weiß.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-9098R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9098R-A750
Lokale Artikelnummer::
BOSSBS-9098R-A750
Beschreibung:
ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. 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 associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7341R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-CY5.5
Lokale Artikelnummer::
BOSSBS-7341R-CY5.5
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-9729R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R-CY5.5
Lokale Artikelnummer::
BOSSBS-9729R-CY5.5
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:
(BOSSBS-9729R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R
Lokale Artikelnummer::
BOSSBS-9729R
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:
(BOSSBS-11130R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11130R-CY7
Lokale Artikelnummer::
BOSSBS-11130R-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 KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(132-0989)
Lieferant:
Palbam
Hersteller-Artikelnummer::
GRW16CMP
Lokale Artikelnummer::
PALBGRW16CMP
Beschreibung:
An der Wand montierte Kleiderständer aus Edelstahl 304 mit elektropolierter Oberfläche.
VE:
1 * 1 ST
Artikel-Nr:
(USBI145105)
Lieferant:
US Biological
Hersteller-Artikelnummer::
145105
Lokale Artikelnummer::
USBI145105
Beschreibung:
Anti-PSTAIR Mouse Monoclonal Antibody [clone: IL-16]
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-12225R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12225R-A750
Lokale Artikelnummer::
BOSSBS-12225R-A750
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 characterised 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 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 ZNF843 gene product has been provisionally designated MGC46336 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12225R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12225R-A680
Lokale Artikelnummer::
BOSSBS-12225R-A680
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 characterised 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 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 ZNF843 gene product has been provisionally designated MGC46336 pending further characterisation.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Suppresses nitric oxide lysis of pancreatic islet cells.
Lieferant:
HERAEUS
Beschreibung:
Address lab’s regular- to medium-throughput blood processing needs with the Thermo Scientific™ HAEMAFlex™ six swinging bucket rotor with 6×550 ml blood bag capacity or, utilising the same bucket system, upgrade to 8×550 ml bags with the Thermo Scientific™ HAEMAFlex™ eight swinging bucket rotor.
Lieferant:
Bohlender
Beschreibung:
Vario 2-part coupling to connect elastic tubing with non-elastic tubing made of PTFE, glass, metal or other plastics.
Artikel-Nr:
(129-0581)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI129-0581
Beschreibung:
Zur sicheren Entsorgung von Laborabfällen wie Pipettenspitzen, Einweg-Petrischalen, Probenröhrchen usw. PP, 40 µm dick, klar, mit oder ohne ‚Biohazard‘-Aufdruck.
VE:
1 * 500 ST
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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