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N-(5-Brom-2-pyridyl)thioharnstoff
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N-(5-Brom-2-pyridyl)thioharnstoff
Artikel-Nr:
(BOSSBS-11945R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A750
Lokale Artikelnummer::
BOSSBS-11945R-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 C12orf52 gene product has been provisionally designated C12orf52 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9944R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9944R-A750
Lokale Artikelnummer::
BOSSBS-9944R-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 C12orf4 gene product has been provisionally designated C12orf4 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9944R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9944R-A680
Lokale Artikelnummer::
BOSSBS-9944R-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 C12orf4 gene product has been provisionally designated C12orf4 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A488
Lokale Artikelnummer::
BOSSBS-8229R-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 FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
EDTA (Ethylendiamintetraessigsäure) ≥99,4% ACS
Lieferant:
Thermo Scientific
Beschreibung:
Triammoniumdodecamolybdophosphat Hydrat
Artikel-Nr:
(H37863.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
H37863.06
Lokale Artikelnummer::
ALFAH37863.06
Beschreibung:
Triphos 97+%
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-0019R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0019R-CY7
Lokale Artikelnummer::
BOSSBS-0019R-CY7
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:
(ACRO365580050)
Lieferant:
Thermo Scientific
Hersteller-Artikelnummer::
365580050
Lokale Artikelnummer::
ACRO365580050
Beschreibung:
α-Brom-2,3-dichlortoluol 99%
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-11698R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-A750
Lokale Artikelnummer::
BOSSBS-11698R-A750
Beschreibung:
Huntingtin yeast partner E is a 458 amino acid single-pass membrane protein. HYPE is thought to interact with Huntingtin, a protein which induces neurodegeneration when mutated. HYPE also contains two tetratricopeptide repeats (TPR), which may be involved in protein-protein interaction. The gene that encodes HYPE is located on chromosome 12, which encodes over 1100 genes within 132 million bases and 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. 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.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD88079-5G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD88079-5G
Lokale Artikelnummer::
BLDPBD88079-5G
Beschreibung:
3-Methylisonicotinsäure 97%
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Isopropyloxazolidine-2,5-dione 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl 5-cyano-2-methoxybenzoate 96%
Artikel-Nr:
(APOSOR3680-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR3680-250MG
Lokale Artikelnummer::
APOSOR3680-250MG
Beschreibung:
7-Chlor-1H-indazol
VE:
1 * 250 mg
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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