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N1-Methylbenzene-1,2-diamine+dihydrochloride
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N1-Methylbenzene-1,2-diamine+dihydrochloride
Artikel-Nr:
(BOSSBS-11003R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-CY3
Lokale Artikelnummer::
BOSSBS-11003R-CY3
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
Lieferant:
Brady
Beschreibung:
FreezerBondz thermal transfer printers labels can be applied to frozen surfaces including glass and polypropylene stored in liquid nitrogen. These labels are on a 1" core, a 'smaller core' than the majority of labels. Recommended printer for these is the BBP11-34L printer.
Artikel-Nr:
(APOSPC10114-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC10114-1G
Lokale Artikelnummer::
APOSPC10114-1G
Beschreibung:
3-Chloro-1-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]-5-(trifluoromethyl)-2(1H)-pyridinone
VE:
1 * 1 g
Artikel-Nr:
(BLDPBD22128-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD22128-25G
Lokale Artikelnummer::
BLDPBD22128-25G
Beschreibung:
1,3-Bis(diphenylphosphino)propan 97%
VE:
1 * 25 g
Artikel-Nr:
(BLDPBD15063-10G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD15063-10G
Lokale Artikelnummer::
BLDPBD15063-10G
Beschreibung:
3,4-Difluorbenzophenon 98%
VE:
1 * 10 g
Artikel-Nr:
(BLDPBD01465655-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01465655-25G
Lokale Artikelnummer::
BLDPBD01465655-25G
Beschreibung:
1,12-Dodecandiol 98+%
VE:
1 * 25 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Pentane-2,3,4-trione 3-oxime
Artikel-Nr:
(BOSSBS-5049R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R
Lokale Artikelnummer::
BOSSBS-5049R
Beschreibung:
Catalyzes the first step in the oxidation of the side chain of sterol intermediates; the 27-hydroxylation of 5-beta-cholestane-3-alpha,7-alpha,12-alpha-triol. Has also a vitamin D3-25-hydroxylase activity.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
(2S)-2-Oxiranylmethanol 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
L(+)-Ascorbinsäure ≥99,5%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2',3'-Difluoracetophenon 97%
Artikel-Nr:
(BOSSBS-9950R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9950R-A750
Lokale Artikelnummer::
BOSSBS-9950R-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 C12orf50 gene product has been provisionally designated C12orf50 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11003R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-A555
Lokale Artikelnummer::
BOSSBS-11003R-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 FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11003R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-A647
Lokale Artikelnummer::
BOSSBS-11003R-A647
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-9952R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9952R-A680
Lokale Artikelnummer::
BOSSBS-9952R-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 C12orf54 gene product has been provisionally designated C12orf54 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9955R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9955R-A680
Lokale Artikelnummer::
BOSSBS-9955R-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 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.
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