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Tetrabutylazanium+trifluoro(3-fluorophenyl)boranuide
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Tetrabutylazanium+trifluoro(3-fluorophenyl)boranuide
Artikel-Nr:
(TCAT613-0151RCH)
Lieferant:
TECAN TRADING
Hersteller-Artikelnummer::
613-0151RCH
Lokale Artikelnummer::
TCAT613-0151RCH
Beschreibung:
Silica-based sorbent with C18 bonding in proprietary coverage.
VE:
1 * 1 ST
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,2,8,8-Tetramethyl-3,6-nonadiyn-5-ol 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1-(2-Morpholinoethyl)-1H-pyrazol-4-boronsäurepinakolester 98%
Artikel-Nr:
(631-1341)
Lieferant:
MENZEL
Hersteller-Artikelnummer::
CB00150RA120
Lokale Artikelnummer::
MENZCB00150RA120
Beschreibung:
Diese Deckgläser sind für <i>in vitro</i>-diagnostische Anwendungen (IVD) geeignet.
VE:
1 * 1.000 ST
Artikel-Nr:
(BLDPBD95372-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD95372-10G
Lokale Artikelnummer::
BLDPBD95372-10G
Beschreibung:
4-Bromresorcin 96%
VE:
1 * 10 g
Lieferant:
DWK Life Sciences
Beschreibung:
Die mit Gummi ausgekleideten Kappen verfügen über einen ungiftigen weißen Styrol-Butadien-Kautschuk-Liner, der sich ideal für die Arbeit mit Zellkulturen eignet.
Artikel-Nr:
(BOSSBS-8578R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8578R-A750
Lokale Artikelnummer::
BOSSBS-8578R-A750
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-13326R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-A488
Lokale Artikelnummer::
BOSSBS-13326R-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 LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13326R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-A750
Lokale Artikelnummer::
BOSSBS-13326R-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 LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8654R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8654R-HRP
Lokale Artikelnummer::
BOSSBS-8654R-HRP
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 FAM81A gene product has been provisionally designated FAM81A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11012R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11012R-HRP
Lokale Artikelnummer::
BOSSBS-11012R-HRP
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-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11012R-FITC
Lokale Artikelnummer::
BOSSBS-11012R-FITC
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Hydroxy-7-methoxycoumarin 98%
Lieferant:
Alfa Aesar
Beschreibung:
1-Naphthol ≥99%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Methyl-2-propanyl-(3S,4R)-3-fluor-4-hydroxy-1-pyrrolidincarboxylat 96%
Lieferant:
SIGMA ALDRICH MICROSCOPY
Beschreibung:
Methyl Green is a triphenylmethane dye which is mainly used in combination with pyronin. It is suitable for the detection of DNA and RNA. Used in the Methyl Green-Pyronin methods to demonstrate DNA and RNA in tissue sections.
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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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