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2-Ethyl-3,5-dimethylpyrazin
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2-Ethyl-3,5-dimethylpyrazin
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Brom-1,3-dimethoxybenzol 98%
Artikel-Nr:
(APOSOR951842-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR951842-25G
Lokale Artikelnummer::
APOSOR951842-25G
Beschreibung:
Methyl 3-(trimethylsilyl)-4-pentenoate 95%
VE:
1 * 25 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Brom-o-toluylsäure
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Brom-1-iod-2-nitrobenzol 99%
Lieferant:
Alfa Aesar
Beschreibung:
2-Brom-4-fluorbenzolsulfonylchlorid ≥97%
Artikel-Nr:
(BLDPBD206397-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD206397-1G
Lokale Artikelnummer::
BLDPBD206397-1G
Beschreibung:
4-Brom-2-nitro-5-(trifluormethyl)anilin 97%
VE:
1 * 1 g
Lieferant:
Thermo Scientific
Beschreibung:
α-Brom-4-chlortoluol 98%
Lieferant:
SI Analytics
Beschreibung:
Reverse flow viscometers calibrated with constant.
Artikel-Nr:
(BOSSBS-11945R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A555
Lokale Artikelnummer::
BOSSBS-11945R-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 C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-FITC
Lokale Artikelnummer::
BOSSBS-11945R-FITC
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
Artikel-Nr:
(BOSSBS-8229R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A750
Lokale Artikelnummer::
BOSSBS-8229R-A750
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 characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11003R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-FITC
Lokale Artikelnummer::
BOSSBS-11003R-FITC
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-11003R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-A488
Lokale Artikelnummer::
BOSSBS-11003R-A488
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Brom-4-nitroanilin
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
4-Brom-o-anisaldehyd 98%
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Diese Baumwolljersey-Handschuhe sind entweder mit einer ¾-Tauchbeschichtung oder einer vollständigen Nitrilbeschichtung erhältlich.
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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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