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1,2-Phenylendiisothiocyanat
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1,2-Phenylendiisothiocyanat
Artikel-Nr:
(APOSOR32008-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR32008-1G
Lokale Artikelnummer::
APOSOR32008-1G
Beschreibung:
N-Ethyl-5-(1-phenoxyethyl)-1H-pyrazole-1-carboxamide 95%
VE:
1 * 1 g
Lieferant:
Thermo Scientific
Beschreibung:
Tri-tert-butylphosphin 95%
Artikel-Nr:
(H51724.03)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
H51724.03
Lokale Artikelnummer::
ALFAH51724.03
Beschreibung:
Methyl-3-brom-5-hydroxybenzoat ≥97%
VE:
1 * 1 g
Lieferant:
Alfa Aesar
Beschreibung:
5-Fluoro-1,3-dimethyl-2-nitrobenzene 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6-Bromo-2-(methylsulphonyl)-1,2,3,4-tetrahydroisoquinoline 95%
Lieferant:
ANSELL HEALTH CARE
Beschreibung:
Dieser Handschuh aus Baumwoll-Interlockstoff mit kompletter PVC-Beschichtung ist ideal für leichte Arbeiten mit langer Tragedauer.
Lieferant:
Alfa Aesar
Beschreibung:
10,12-Pentacosadiinsäure ≥98%
Artikel-Nr:
(BRDY065666)
Lieferant:
Brady
Hersteller-Artikelnummer::
065666
Lokale Artikelnummer::
BRDY065666
Beschreibung:
These single-piece, easy to use ball valve lockouts are the ideal tool for securing quarter-turn ball valves in the OFF position.
VE:
1 * 1 ST
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Tris[(trifluoromethyl)sulphonyl]methane
Artikel-Nr:
(BOSSBS-0019R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0019R-A680
Lokale Artikelnummer::
BOSSBS-0019R-A680
Beschreibung:
Acts as a cytokine involved in enhancing production of interferon-gamma and interleukin-12 and reducing production of interleukin-10 and is essential in the pathway that leads to type I immunity (By similarity).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-3842R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3842R-A350
Lokale Artikelnummer::
BOSSBS-3842R-A350
Beschreibung:
EIF3S3 binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA. It associates with the p170 subunit of EIF3. The EIF3 is composed of at least 12 different subunits.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A488
Lokale Artikelnummer::
BOSSBS-11945R-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 C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9953R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9953R-A750
Lokale Artikelnummer::
BOSSBS-9953R-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 C12orf61 gene product has been provisionally designated C12orf61 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9947R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9947R-A680
Lokale Artikelnummer::
BOSSBS-9947R-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 C12orf40 gene product has been provisionally designated C12orf40 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9945R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9945R-A680
Lokale Artikelnummer::
BOSSBS-9945R-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 C12orf24 gene product has been provisionally designated C12orf24 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9955R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9955R-A750
Lokale Artikelnummer::
BOSSBS-9955R-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 LOC387856 gene product has been provisionally designated LOC387856 pending further characterisation.
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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