Suche >
4-Hydroxy-2,3,5-trifluorobenzoic+acid
Drucken
Sie suchten nach:
140 079 results were found
4-Hydroxy-2,3,5-trifluorobenzoic+acid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Ethyl-2,3,4-trifluorbenzoat
Lieferant:
Merck
Beschreibung:
Magnesiumhydroxidcarbonat leicht Ph. Eur., BP, reinst, SAFC®
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl-2,4,6-trifluorbenzoat 98%
Lieferant:
Merck
Beschreibung:
Magnesiumhydroxidcarbonat schwer (Parteck® Mg DC), EMPROVE® ESSENTIAL Ph. Eur., BP, USP, JP, E504, SAFC®
Artikel-Nr:
(COBBBB-8340-1G)
Lieferant:
COMBI-BLOCKS
Hersteller-Artikelnummer::
BB-8340-1G
Lokale Artikelnummer::
COBBBB-8340-1G
Beschreibung:
2,3,5-Trichlorphenylboronsäure
VE:
1 * 1 g
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(BOSSBS-13623R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-A555
Lokale Artikelnummer::
BOSSBS-13623R-A555
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13623R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-CY7
Lokale Artikelnummer::
BOSSBS-13623R-CY7
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13623R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-A647
Lokale Artikelnummer::
BOSSBS-13623R-A647
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13623R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-HRP
Lokale Artikelnummer::
BOSSBS-13623R-HRP
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13623R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-A488
Lokale Artikelnummer::
BOSSBS-13623R-A488
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13623R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-FITC
Lokale Artikelnummer::
BOSSBS-13623R-FITC
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
2,3,5-Triiodbenzoesäure, Sigma-Aldrich®
Artikel-Nr:
(SIAL357782-1G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
357782-1G
Lokale Artikelnummer::
SIAL357782-1G
Beschreibung:
2,3,5-Trichlorbenzoesäure, Sigma-Aldrich®
VE:
1 * 1 g
Artikel-Nr:
(1.05829.9040)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.05829.9040
Lokale Artikelnummer::
MERP1.05829.9040
Beschreibung:
Magnesiumhydroxidcarbonat schwer Ph. Eur., BP, USP, E504, reinst pH 10.5 (50 g/l, H₂O, 20 °C), SAFC®
VE:
1 * 40 kg
Artikel-Nr:
(BOSSBS-13623R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-CY3
Lokale Artikelnummer::
BOSSBS-13623R-CY3
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13623R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13623R-CY5
Lokale Artikelnummer::
BOSSBS-13623R-CY5
Beschreibung:
TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
VE:
1 * 100 µl
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.
Dieses Produkt ist nicht mehr verfügbar. Bitte kontaktieren Sie den VWR Kundenservice.
|
|||||||||
Listenansicht
