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2-(4-Chlorophenyl)oxazole-4-carboxylic+acid
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2-(4-Chlorophenyl)oxazole-4-carboxylic+acid
Lieferant:
Alfa Aesar
Beschreibung:
α,α-Dimethylpropiophenon ≥98%
Lieferant:
Alfa Aesar
Beschreibung:
Diethyladipat ≥99%
Artikel-Nr:
(BOSSBS-9023R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R-CY3
Lokale Artikelnummer::
BOSSBS-9023R-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. alternatively splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9023R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R-CY7
Lokale Artikelnummer::
BOSSBS-9023R-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. alternatively splicing events.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9023R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R-CY5.5
Lokale Artikelnummer::
BOSSBS-9023R-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. alternatively splicing events.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
Lopinavir 98%
Artikel-Nr:
(BOSSBS-13132R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13132R-A750
Lokale Artikelnummer::
BOSSBS-13132R-A750
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-9629R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9629R-FITC
Lokale Artikelnummer::
BOSSBS-9629R-FITC
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:
(ABCAAB270294-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB270294-100
Lokale Artikelnummer::
ABCAAB270294-100
Beschreibung:
Anti-Cadherin 16 Rabbit Monoclonal Antibody [clone: CDH16/1532R]
VE:
1 * 100 µG
 This is a MarketSource item. Additional charges may apply
Lieferant:
Avantor Fluid Handling
Beschreibung:
Für generelle Anwendungen geeignet.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Methoxydiphenylamin 98%
Artikel-Nr:
(APOSOR313010-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR313010-1G
Lokale Artikelnummer::
APOSOR313010-1G
Beschreibung:
4-Acetylpyrazole
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Vinylpyrrolidone
Artikel-Nr:
(BOSSBS-9629R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9629R-A488
Lokale Artikelnummer::
BOSSBS-9629R-A488
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:
Cayman Chemical
Beschreibung:
2-Methyl-4-phenylthiazol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-(Bromomethyl)quinoline
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.
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