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4,4-Dimethylcyclohexa-1,5-dienylborons\u00E4ure+Mononatriumsalz
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4,4-Dimethylcyclohexa-1,5-dienylborons\u00E4ure+Mononatriumsalz
Artikel-Nr:
(ABCAAB312759-100UL)
Lieferant:
Abcam
Beschreibung:
Anti-Cytokeratin 15 Rabbit Monoclonal Antibody [clone: EPR1614Y] (Alexa Fluor® 568)
VE:
1 * 100 µl
Artikel-Nr:
(ABCAAB187160-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB187160-100
Lokale Artikelnummer::
ABCAAB187160-100
Beschreibung:
Anti-15-PGDH Rabbit Monoclonal Antibody [clone: EPR14332]
VE:
1 * 100 µl
 This is a MarketSource item. Additional charges may apply
Lieferant:
Alfa Aesar
Beschreibung:
Hexafluorglutarsäure ≥98%
Lieferant:
VWR Collection
Beschreibung:
Gewichte aus antimagnetischem und poliertem Edelstahl. Geeignet für elektronische Präzisionswaagen mit mittlerer Auflösung. Gewichte über 20 g weisen Aussparungen für die Justierung auf.
Lieferant:
Alfa Aesar
Beschreibung:
Formylglycin 98%
Lieferant:
EBRO
Beschreibung:
These data loggers are high-precision temperature and pressure loggers designed for process validation in steam sterilisers, batch control, and pharmaceutical applications. With a wide temperature and pressure range and high accuracy, they provide reliable data logging for critical monitoring processes in sterilisation, healthcare, production, and pharmaceutical environments, ensuring accurate validation and quality control.
Artikel-Nr:
(ABCAAB305208-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB305208-100
Lokale Artikelnummer::
ABCAAB305208-100
Beschreibung:
Anti-CX3CR1 Rabbit Monoclonal Antibody [clone: EPR22354-15] (Alexa Fluor® 647)
VE:
1 * 100 µl
This is a MarketSource item. Additional charges may apply
Lieferant:
Spectrum Chemical
Beschreibung:
Cetostearyl Alcohol, NF is used as a stabiliser and opacifying agent.
Artikel-Nr:
(BOSSBS-8578R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-HRP
Lokale Artikelnummer::
BOSSBS-8578R-HRP
Beschreibung:
GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8578R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-CY5.5
Lokale Artikelnummer::
BOSSBS-8578R-CY5.5
Beschreibung:
GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8578R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-A647
Lokale Artikelnummer::
BOSSBS-8578R-A647
Beschreibung:
GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Amino-2-pyridincarbonitril 98%
Artikel-Nr:
(620-0940)
Lieferant:
VWR Collection
Lokale Artikelnummer::
VWRI620-0940
Beschreibung:
Diese quecksilberfreien Thermometer sind einzeln kalibriert und dienen zur Überprüfung von Probentemperaturen. Zur Verwendung in Gefriergeräten, Kühlschränken, Inkubatoren, Öfen und Blutbanken.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-11012R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11012R-A488
Lokale Artikelnummer::
BOSSBS-11012R-A488
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11012R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11012R-A750
Lokale Artikelnummer::
BOSSBS-11012R-A750
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterisation.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
3,4-Dimethylthiophen 97%
Preis auf Anfrage
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.
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.
Dieses Produkt wurde von Ihrer Organisation gesperrt. Bitte kontaktieren Sie Ihren Einkauf für weitere Informationen.
Dieses Produkt ist Ersatz für den von Ihnen gewünschten Artikel.
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