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N1-Methylbenzene-1,2-diamine+dihydrochloride
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N1-Methylbenzene-1,2-diamine+dihydrochloride
Lieferant:
Thermo Scientific
Beschreibung:
Triammoniumdodecamolybdophosphat Hydrat
Artikel-Nr:
(BLDPBD273105-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD273105-250MG
Lokale Artikelnummer::
BLDPBD273105-250MG
Beschreibung:
4-Isopropyloxazolidine-2,5-dione 95%
VE:
1 * 250 mg
Artikel-Nr:
(442-1219)
Lieferant:
SI Analytics
Hersteller-Artikelnummer::
285402198
Lokale Artikelnummer::
SCOI285402198
Beschreibung:
Diese Kapillarviskosimeter sind für automatische Messungen in Routineanwendungen kalibriert.
VE:
1 * 1 ST
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:
(590-0178)
Lieferant:
Bohlender
Hersteller-Artikelnummer::
M506-03
Lokale Artikelnummer::
BOHLM506-03
Beschreibung:
Filtergehäuse aus PP mit Anschluss (Gewinde GL14) passend für b.safe Waste Caps.
Deckel mit Belüftungsöffnungen und Wechselanzeige mit Beschriftungsfeld zur Überwachung der Standzeit. Füllung aus Aktivkohle zur Adsorption von Lösemitteln.
VE:
1 * 2 ST
Lieferant:
Hichrom Limited
Beschreibung:
Vydac TP ist die erste im Vydac-Sortiment entwickelte Reihe weitporiger Medienphasen und ist der Branchenstandard für Peptid- und Proteintrennungen. Die großen Poren des 300-Å-TP-Silica ermöglichen Polypeptidmolekülen vollständigen Zugang zum Inneren der Silica-Poren.
Artikel-Nr:
(BLDPBD33328-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD33328-10G
Lokale Artikelnummer::
BLDPBD33328-10G
Beschreibung:
2'-Aminoacetanilid 98%
VE:
1 * 10 g
Artikel-Nr:
(BOSSBS-11822R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11822R-A680
Lokale Artikelnummer::
BOSSBS-11822R-A680
Beschreibung:
CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyses 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-8229R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-FITC
Lokale Artikelnummer::
BOSSBS-8229R-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 FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9950R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9950R-A680
Lokale Artikelnummer::
BOSSBS-9950R-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 C12orf50 gene product has been provisionally designated C12orf50 pending further characterisation.
VE:
1 * 100 µl
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:
APOLLO SCIENTIFIC
Beschreibung:
1,3-Bis(diphenylphosphino)propan 97%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Optical brightener for plastics (PP, ABS, EVA, PS and PC) and fibre (polyester fibres and PP fibres).
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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