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cis-1,2-Cyclopentandiol
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cis-1,2-Cyclopentandiol
Lieferant:
Thermo Fisher Scientific
Beschreibung:
Aluminium. Kann mit Farbcodierungsstreifen markiert werden.
Lieferant:
Bohlender
Beschreibung:
Bolzen und Spreizscheiben komplett aus PTFE, hauptsächliche Verwendung mit Halbmond-Rohrblättern mit Doppelnut.
Artikel-Nr:
(APOSPC1431-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC1431-1G
Lokale Artikelnummer::
APOSPC1431-1G
Beschreibung:
4-(Difluoromethoxy)benzeneboronic acid
VE:
1 * 1 g
Artikel-Nr:
(APOSOR4648-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR4648-25G
Lokale Artikelnummer::
APOSOR4648-25G
Beschreibung:
4-(Trimethylsilyloxy)benzaldehyd 97%
VE:
1 * 25 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-(Bromomethyl)-4-fluorobenzaldehyde
Artikel-Nr:
(ACRO456241000)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
456241000
Lokale Artikelnummer::
ACRO456241000
Beschreibung:
Capecitabin 99%
VE:
1 * 100 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Diphosphate Salt, >99%
Artikel-Nr:
(ACRO166560250)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
166560250
Lokale Artikelnummer::
ACRO166560250
Beschreibung:
4-Chlorphenylisocyanat 98%
VE:
1 * 25 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Chlor-4-hydroxypyridin
Lieferant:
Thermo Scientific
Beschreibung:
Tetrabromphenolblau, rein
Artikel-Nr:
(BOSSBS-11003R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-HRP
Lokale Artikelnummer::
BOSSBS-11003R-HRP
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9948R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9948R-A750
Lokale Artikelnummer::
BOSSBS-9948R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf42 gene product has been provisionally designated C12orf42 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A680
Lokale Artikelnummer::
BOSSBS-11945R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A647
Lokale Artikelnummer::
BOSSBS-8229R-A647
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A555
Lokale Artikelnummer::
BOSSBS-8229R-A555
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A647
Lokale Artikelnummer::
BOSSBS-11945R-A647
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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