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1-(2-Fluorophenyl)-4-oxocyclohexanecarboxylic+acid
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1-(2-Fluorophenyl)-4-oxocyclohexanecarboxylic+acid
Artikel-Nr:
(BOSSBS-11589R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11589R-CY3
Lokale Artikelnummer::
BOSSBS-11589R-CY3
Beschreibung:
The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxC5 is a 222 amino acid protein that localizes to the nucleus and contains one homeobox DNA-binding domain. Existing as multiple alternatively spliced isoforms, HoxC5 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. The gene encoding HoxC5 maps to a cluster of Hox proteins on chromosome 12 that are essential for morphogenesis. 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.
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD11148-100G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD11148-100G
Lokale Artikelnummer::
BLDPBD11148-100G
Beschreibung:
3',4'-Dihydroxyacetophenon 98%
VE:
1 * 100 g
Artikel-Nr:
(BLDPBD204427-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD204427-100MG
Lokale Artikelnummer::
BLDPBD204427-100MG
Beschreibung:
1-(4-Aminophenyl)-4-piperidinol 97%
VE:
1 * 100 mg
Artikel-Nr:
(BLDPBD21064-1000G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD21064-1000G
Lokale Artikelnummer::
BLDPBD21064-1000G
Beschreibung:
10-Bromdecansäure 95%
VE:
1 * 1.000 g
Lieferant:
Merck
Beschreibung:
Titriplex® III ACS, ISO, Reag. Ph. Eur. analytisches Reagens, Supelco®
Lieferant:
Thermo Scientific
Beschreibung:
2,3-Dichlor-5,6-dicyan-p-benzochinon 98%
Artikel-Nr:
(HACH4565500)
Lieferant:
Hach
Hersteller-Artikelnummer::
4565500
Lokale Artikelnummer::
HACH4565500
Beschreibung:
Bi-metallic dial gauge 0 to 200 °C ±1%. Two degree divisions.
VE:
1 * 1 ST
Artikel-Nr:
(HI21-20-033-12)
Lieferant:
HICHROM GAS CHROMATOGRAPHY
Lokale Artikelnummer::
HIGCHI21-20-033-12
Beschreibung:
Proprietäre stationäre Phase mit niedriger Polarität und geringer Blutung; Gute Wahl für Pestizide, Herbizide, polychlorierte Biphenyle (PCBs) und polyaromatische Kohlenwasserstoffe (PAKs). Ideal für GC/MS-Anwendungen und auch eine ausgezeichnete Wahl als Bestätigungssäule für halbflüchtige Umweltanalysen.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-11003R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-HRP
Lokale Artikelnummer::
BOSSBS-11003R-HRP
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-9948R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9948R-A750
Lokale Artikelnummer::
BOSSBS-9948R-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 C12orf42 gene product has been provisionally designated C12orf42 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A680
Lokale Artikelnummer::
BOSSBS-11945R-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 C12orf52 gene product has been provisionally designated C12orf52 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A647
Lokale Artikelnummer::
BOSSBS-8229R-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 FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A555
Lokale Artikelnummer::
BOSSBS-8229R-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 FAM101A gene product has been provisionally designated FAM101A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A647
Lokale Artikelnummer::
BOSSBS-11945R-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 C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11945R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A350
Lokale Artikelnummer::
BOSSBS-11945R-A350
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
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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