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2-Fluor-5-nitro-6-picolin
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2-Fluor-5-nitro-6-picolin
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-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
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
Lieferant:
Alfa Aesar
Beschreibung:
Stabilized with 100 ppm 4-methoxyphenol
Artikel-Nr:
(41771.36)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
41771.36
Lokale Artikelnummer::
ALFA41771.36
Beschreibung:
Phthalsäureanhydrid 99,0-100,2% ACS
VE:
1 * 500 g
Lieferant:
SI Analytics
Beschreibung:
Reverse flow viscometers calibrated with constant.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-(Trifluormethoxy)benzoesäure 97%
Artikel-Nr:
(BOSSBS-6798R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6798R-CY3
Lokale Artikelnummer::
BOSSBS-6798R-CY3
Beschreibung:
Calpains are a family of cytosolic calcium activated cysteine proteases involved in a variety of cellular processes including apoptosis, cell division, modulation of integrin and cytoskeletal interactions, and synaptic plasticity. Calpain 12 was first described in the mouse, most strongly in the skin, and maps to mouse chromosome 7. Isoforms differ in the carboxyterminal ends, ending with aberrant domain III and lacking domain IV. Domains in the large subunit include the amino terminal domain I, the proteinase domain II, domain III, and the EF hand domain IV, making Calpain 12 most similar to calpains 1 and 2.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR12650-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR12650-250MG
Lokale Artikelnummer::
APOSOR12650-250MG
Beschreibung:
4-(4-Pyridyl)benzaldehyd 98%
VE:
1 * 250 mg
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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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