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4-Carboxy-2-nitrophenylboronsäure
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96 603 results were found
4-Carboxy-2-nitrophenylboronsäure
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
Lieferant:
Avantor Fluid Handling
Beschreibung:
Für generelle Anwendungen geeignet.
Artikel-Nr:
(BOSSBS-13132R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13132R-A647
Lokale Artikelnummer::
BOSSBS-13132R-A647
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-7341R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-CY5
Lokale Artikelnummer::
BOSSBS-7341R-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. The C16orf72 gene product has been provisionally designated C16orf72 pending further characterization.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-(Bromomethyl)quinoline
Lieferant:
SWANN MORTON
Beschreibung:
Sterile and non sterile scalpel blades made from carbon steel or stainless steel.
Lieferant:
Bohlender
Beschreibung:
Fitting made of PTFE, white.
Artikel-Nr:
(APOSPC10318-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC10318-1G
Lokale Artikelnummer::
APOSPC10318-1G
Beschreibung:
Pentafluorphenylphenylmethansulfonat
VE:
1 * 1 g
Artikel-Nr:
(B20395.03)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
B20395.03
Lokale Artikelnummer::
ALFAB20395.03
Beschreibung:
2,4,5-Trifluorphenol ≥94%
VE:
1 * 1 g
Artikel-Nr:
(1.14438.0001)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.14438.0001
Lokale Artikelnummer::
MERC1.14438.0001
Beschreibung:
Testsätze für die schnelle, halbquantitative Analyse vor Ort, ohne den aufwendigen Transport ins Labor. Die Ergebnisse sind direkt vor Ort verfügbar. Die einfache, anwenderfreundliche Bedienungsanleitung gewährleistet eine Anwendung ohne zusätzliche Schulungen.
VE:
1 * 500 Tests
Artikel-Nr:
(AGLSG9700A)
Lieferant:
AGILENT
Hersteller-Artikelnummer::
G9700A
Lokale Artikelnummer::
AGLSG9700A
Beschreibung:
The Agilent NGS FFPE QC kit is a qPCR-based assay that enables functional DNA quality assessment of input DNA prior to preparation of next generation sequencing (NGS) libraries.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-7341R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-A750
Lokale Artikelnummer::
BOSSBS-7341R-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 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 characterisation.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2'-Methylacetophenon
Artikel-Nr:
(BOSSBS-7341R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7341R-HRP
Lokale Artikelnummer::
BOSSBS-7341R-HRP
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
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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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