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[2-(4-Bromobenzyl)thiazol-4-y]acetic+acid
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[2-(4-Bromobenzyl)thiazol-4-y]acetic+acid
Lieferant:
Alfa Aesar
Beschreibung:
Perfluoro(methyldecalin) mixture of 1- and 2-isomers (∼1:1) ≥85%, tech.
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
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
Lieferant:
Avantor Fluid Handling
Beschreibung:
Particulate will not adhere to liner.
Artikel-Nr:
(590-0215)
Lieferant:
Bohlender
Hersteller-Artikelnummer::
M542-01
Lokale Artikelnummer::
BOHLM542-01
Beschreibung:
Innenkontur passend zur Außenkontur der b.safe Fittings für Kapillarschläuche.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-13132R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13132R-A680
Lokale Artikelnummer::
BOSSBS-13132R-A680
Beschreibung:
FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. 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-9023R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R-CY5
Lokale Artikelnummer::
BOSSBS-9023R-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. alternatively splicing events.
VE:
1 * 100 µl
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:
(BELAF188601316)
Lieferant:
Bel-Art Products, a Part of SP
Hersteller-Artikelnummer::
F188601316
Lokale Artikelnummer::
BELAF188601316
Beschreibung:
PP, weiß
VE:
1 * 1 ST
Lieferant:
Avantor
Beschreibung:
Für Robotersysteme Hamilton Microlab Star und Nimbus geeignet. Als leitfähige Version, mit oder ohne Filter, mit CE-IVD/CE-Kennzeichnung für Anwendungen in der klinischen Diagnostik verfügbar.
Lieferant:
VWR Collection
Beschreibung:
Gewichte aus massivem, antimagnetischem und poliertem Edelstahl. Für hochauflösende, elektronische Waagen geeignet.
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:
(BOSSBS-13132R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13132R-FITC
Lokale Artikelnummer::
BOSSBS-13132R-FITC
Beschreibung:
FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. 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:
(BRDY132474)
Lieferant:
Brady
Hersteller-Artikelnummer::
132474
Lokale Artikelnummer::
BRDY132474
Beschreibung:
High temperature polyimide labels to withstand aggressive cleaning processes.
VE:
1 * 1 Rolle
Artikel-Nr:
(BOSSBS-9023R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R-A555
Lokale Artikelnummer::
BOSSBS-9023R-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. alternatively splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12225R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12225R-CY7
Lokale Artikelnummer::
BOSSBS-12225R-CY7
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
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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