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1,6-Anhydro-\\u03B2-D-mannopyranose
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16 904 results were found
1,6-Anhydro-\\u03B2-D-mannopyranose
Artikel-Nr:
(BOSSBS-7341R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-A555
Lokale Artikelnummer::
BOSSBS-7341R-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 C16orf72 gene product has been provisionally designated C16orf72 pending further characterization.
VE:
1 * 100 µl
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:
(BRDY813853)
Lieferant:
Brady
Hersteller-Artikelnummer::
813853
Lokale Artikelnummer::
BRDY813853
Beschreibung:
These Hazwik pillows are used for absorbing spills and leaking liquids in tight spaces.
VE:
1 * 16 ST
Lieferant:
Thermo Scientific
Beschreibung:
Curcumin 98+% (mixture of curcumin, demethoxycurcumin, and bisdemethoxycurcumin)
Artikel-Nr:
(APOSOR317147-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR317147-1G
Lokale Artikelnummer::
APOSOR317147-1G
Beschreibung:
7-Aza-spiro[3.5]nonane hydrochloride
VE:
1 * 1 g
Artikel-Nr:
(1.00307.1000)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.00307.1000
Lokale Artikelnummer::
MERC1.00307.1000
Beschreibung:
Bromwasserstoff 47%, EMSURE® ISO zur Analyse, Supelco®
VE:
1 * 1 L
Artikel-Nr:
(BRDY034052)
Lieferant:
Brady
Hersteller-Artikelnummer::
034052
Lokale Artikelnummer::
BRDY034052
Beschreibung:
These write-on labels provide easy identification for calibration, testing, and repair of tools and equipment.
VE:
1 * 1 KIT
Artikel-Nr:
(BOSSBS-8405R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8405R-A680
Lokale Artikelnummer::
BOSSBS-8405R-A680
Beschreibung:
GFOD2 is a 385 amino acid secreted protein of the extracellular matrix that belongs to the gfo/idh/mocA family. Existing as two alternatively spliced isoforms, GFOD2 enhances matrix assembly and is encoded by a gene that maps to human chromosome 16q22.1. Chromosome 16 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 also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Pure Al₂O₃<sub> </sub>Aluminium oxide AL23.
Artikel-Nr:
(BOSSBS-9729R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9729R-A750
Lokale Artikelnummer::
BOSSBS-9729R-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. The FAM96B gene product has been provisionally designated FAM96B pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(442-0495)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI442-0495
Beschreibung:
<B>PTFE</B>-ummantelter Alnico V-Magnetkern. Glatte Oberfläche. Für Rühraufgaben in Reagenzgläsern, Zentrifugengläsern und Mikro-Vials. Die Flügel können bei Bedarf selbst auf die benötigte Größe zugeschnitten werden.
VE:
1 * 10 ST
Artikel-Nr:
(BOSSBS-9037R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9037R
Lokale Artikelnummer::
BOSSBS-9037R
Beschreibung:
Proteins containing PDZ domains have been shown frequently to bind the C-termini of transmembrane receptors or ion channels. They have also been shown to bind to other PDZ domain proteins and could possibly be involved in intracellular signalling. PDZK3 contains six PDZ domains and shares sequence similarity with pro-interleukin-16 (pro-IL-16). Like pro-IL-16, the encoded protein localizes to the endoplasmic reticulum and is thought to be cleaved by a caspase to produce a secreted peptide containing two PDZ domains. In addition, the PDZK3 gene is upregulated in primary prostate tumors and may be involved in the early stages of prostate tumorigenesis.
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.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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