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2-Benzyloxy-5-pyrimidinboronsäurepinakolester
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2-Benzyloxy-5-pyrimidinboronsäurepinakolester
Artikel-Nr:
(BLDPBD28569-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD28569-25G
Lokale Artikelnummer::
BLDPBD28569-25G
Beschreibung:
6-(Trifluormethyl)nicotinaldehyd 98%
VE:
1 * 25 g
Lieferant:
Hach
Beschreibung:
These lightweight samplers with low power requirements (12 VDC) have been designed for easy mobility.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1,2,3,4-Tetrahydro-2-naphthoic acid 96%
Artikel-Nr:
(APOSOR346595-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR346595-1G
Lokale Artikelnummer::
APOSOR346595-1G
Beschreibung:
3-Brompyrazolo[1,5-a]pyridin 95+%
VE:
1 * 1 g
Lieferant:
Cayman Chemical
Beschreibung:
Q-VD-OPH is a broad-spectrum caspase inhibitor, blocking caspases-3, -7, -8, -9, -10, and -12 and inhibiting apoptosis when used at 10 µm. It more effectively inhibits apoptosis and is much less cytotoxic than Z-VAD-FMK and Boc-D-FMK.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-{[3-(Trifluoromethyl)pyridin-2-yl]oxy}benzoic acid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
D-Glucoronic acid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-(3-Chloro-2-fluorophenyl)propionic acid 97%
Artikel-Nr:
(BOSSBS-3842R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3842R-CY3
Lokale Artikelnummer::
BOSSBS-3842R-CY3
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-3842R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3842R-CY5.5
Lokale Artikelnummer::
BOSSBS-3842R-CY5.5
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-11822R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A555
Lokale Artikelnummer::
BOSSBS-11822R-A555
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
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
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.
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