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1,2-Propylendiamin
Artikel-Nr:
(MAXA2053016)
Lieferant:
MAXX
Hersteller-Artikelnummer::
2053016
Lokale Artikelnummer::
MAXA2053016
Beschreibung:
Ein tragbarer, batteriebetriebener und kompakter automatischer Wasserprobennehmer mit einem Vakuumsammelsystem mit Membranpumpe. Das Standardmodell hat einen integrierten isolierten Behälter und Verteiler für 24×1-l-PE-Flaschen; die Probenahme erfolgt über die programmierbare Mikroprozessorsteuerung.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-9023R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9023R-A680
Lokale Artikelnummer::
BOSSBS-9023R-A680
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. 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
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-13197R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-A680
Lokale Artikelnummer::
BOSSBS-13197R-A680
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-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-FITC
Lokale Artikelnummer::
BOSSBS-13197R-FITC
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-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-A488
Lokale Artikelnummer::
BOSSBS-13197R-A488
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:
(BIND9010-0341)
Lieferant:
Binder
Hersteller-Artikelnummer::
9010-0341
Lokale Artikelnummer::
BIND9010-0341
Beschreibung:
Die Avantgarde.Line Wärme- und Trockenschränke mit natürlichem Luftwechsel bieten Qualität und Prozesssicherheit. Mit einem breiten Temperaturbereich bis 300 °C sind diese Trockenschränke universell einsetzbar. Kurze Aufheizzeiten und hohe Leistungsreserven sind ideal für Anwendungen in Wissenschaft, Forschung und Industrie. Die APT.line™ Vorwärmekammertechnologie sorgt für eine homogene Temperaturverteilung, hervorragende Temperaturgenauigkeit und geringe Schwankungen. Geräte von bis zu 115 Litern können aufeinandergestapelt werden um Platz zu sparen. Die Geräte verfügen über eine 60 mm-Isolierung, die den Energieverbrauch senkt und die Leistung steigert. Alle Modelle verfügen über eine Edelstahlkammer mit einem ergonomischen Türöffnungssystem.
VE:
1 * 1 ST
Artikel-Nr:
(BIND9010-0301)
Lieferant:
Binder
Hersteller-Artikelnummer::
9010-0301
Lokale Artikelnummer::
BIND9010-0301
Beschreibung:
Die Avantgarde.Line Wärme- und Trockenschränke mit Umluft und erweiterten Zeitfunktionen bieten Qualität und Prozesssicherheit. Mit einem breiten Temperaturbereich bis 300 °C sind diese Trockenschränke universell einsetzbar. Kurze Aufheizzeiten und hohe Leistungsreserven sind ideal für Anwendungen in Wissenschaft, Forschung und Industrie. Die APT.line™ Vorwärmekammertechnologie sorgt für eine homogene Temperaturverteilung, hervorragende Temperaturgenauigkeit und geringe Schwankungen. Geräte von bis zu 115 Litern können aufeinandergestapelt werden um Platz zu sparen. Die Geräte verfügen über eine 60 mm-Isolierung, die den Energieverbrauch senkt und die Leistung steigert. Alle Modelle verfügen über eine Edelstahlkammer mit einem ergonomischen Türöffnungssystem.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-13197R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13197R-CY5
Lokale Artikelnummer::
BOSSBS-13197R-CY5
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:
(732-3991)
Lieferant:
AGILENT
Hersteller-Artikelnummer::
G2992AA
Lokale Artikelnummer::
AGLSG2992AA
Beschreibung:
Economic, entry-level system for the analysis of up to 16 DNA and RNA samples per run.
VE:
1 * 1 ST
Artikel-Nr:
(ABCAAB315897-1ML)
Lieferant:
Abcam
Beschreibung:
Anti-SNX27 Rabbit Monoclonal Antibody [clone: EPR28130-16]
VE:
1 * 1 mL
New Product
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:
(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:
(PRSIXW-7526)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
XW-7526
Lokale Artikelnummer::
PRSIXW-7526
Beschreibung:
Regulator of G-protein signalling 16 , RGS16. This protein negatively regulates G protein-coupled receptor signalling.
VE:
1 * 50 µG
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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