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5-(4-Hydroxyphenyl)thiophene-2-carboxylic+acid
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5-(4-Hydroxyphenyl)thiophene-2-carboxylic+acid
Artikel-Nr:
(BOSSBS-11002R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11002R
Lokale Artikelnummer::
BOSSBS-11002R
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-8229R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-CY5
Lokale Artikelnummer::
BOSSBS-8229R-CY5
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)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R
Lokale Artikelnummer::
BOSSBS-8229R
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:
1,12-Diaminododecan ≥98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Amino-PEG12-acid
Artikel-Nr:
(BLDPBD218863-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD218863-250MG
Lokale Artikelnummer::
BLDPBD218863-250MG
Beschreibung:
6-Bromo-1H-pyrazolo[4,3-c]pyridine 97%
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,4-Difluorbenzophenon 98%
Artikel-Nr:
(BRDY065666)
Lieferant:
Brady
Hersteller-Artikelnummer::
065666
Lokale Artikelnummer::
BRDY065666
Beschreibung:
These single-piece, easy to use ball valve lockouts are the ideal tool for securing quarter-turn ball valves in the OFF position.
VE:
1 * 1 ST
Lieferant:
Alfa Aesar
Beschreibung:
3',4'-Dimethoxyacetophenon ≥98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
cis-tert-Butyl 3-phenylaziridine-2-carboxylate
Artikel-Nr:
(APOSOR316052-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR316052-1G
Lokale Artikelnummer::
APOSOR316052-1G
Beschreibung:
tert-Butyl (R)-(-)-2-Hydroxy-3,3-Dimethylbutyrate
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Niob(V)chlorid 99,9%
Artikel-Nr:
(APOSOR920675-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR920675-5G
Lokale Artikelnummer::
APOSOR920675-5G
Beschreibung:
2-(4-(Methoxycarbonyl)phenyl)acetic acid 98%
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-11698R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-A350
Lokale Artikelnummer::
BOSSBS-11698R-A350
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 1,100 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:
(BLDPBD00767731-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD00767731-25G
Lokale Artikelnummer::
BLDPBD00767731-25G
Beschreibung:
Lithiumstearat 98%
VE:
1 * 25 g
Lieferant:
Alfa Aesar
Beschreibung:
4-Methylmorpholine N-oxide monohydrate is used as a solvent to prepare cellulose fibers. It is an oxidant and involved in the catalytic OsO4 oxidation of olefins to cis-1,2-diols. It is also involved in ruthenium catalyzed oxidation of alcohols to aldehydes and ketones.
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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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