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(\u00B1)-1,2-Pentandiol
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(\u00B1)-1,2-Pentandiol
Artikel-Nr:
(BOSSBS-11003R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-A350
Lokale Artikelnummer::
BOSSBS-11003R-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 FAM62A gene product has been provisionally designated FAM62A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9951R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9951R-A750
Lokale Artikelnummer::
BOSSBS-9951R-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 C12orf53 gene product has been provisionally designated C12orf53 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9947R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9947R-A750
Lokale Artikelnummer::
BOSSBS-9947R-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 C12orf40 gene product has been provisionally designated C12orf40 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9946R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9946R-A680
Lokale Artikelnummer::
BOSSBS-9946R-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 C12orf29 gene product has been provisionally designated C12orf29 pending further characterisation.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
(R)-(-)-sec-Butylamin 99%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1H-Pyrrolo[2,3-b]pyridine-4-carbaldehyde 95%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-[2-Methyl-5-(trifluoromethyl)phenyl]propionic acid 98%
Artikel-Nr:
(BOSSBS-5049R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R-FITC
Lokale Artikelnummer::
BOSSBS-5049R-FITC
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
Artikel-Nr:
(COWI001.212)
Lieferant:
COWIE
Hersteller-Artikelnummer::
001.212
Lokale Artikelnummer::
COWI001.212
Beschreibung:
Plain PTFE magnetic stirring bars have similar performance to cylindrical bars, but provide more turbulence at low speeds.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-6143R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6143R
Lokale Artikelnummer::
BOSSBS-6143R
Beschreibung:
May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro).
VE:
1 * 100 µl
Lieferant:
DWK Life Sciences
Beschreibung:
Diese Gewindefläschchen bestehen aus klarem und braunem Borosilikatglas (Typ 1). Aufgrund des innovativen Designs sitzt der eingeführte Mikroeinsatz genau in der Mitte des Fläschchens.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
6-Azaspiro[2.5]octan-4-one hydrochloride
Artikel-Nr:
(APOSOR370054-100MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR370054-100MG
Lokale Artikelnummer::
APOSOR370054-100MG
Beschreibung:
5-Acetyl-5-azaspiro[2.4]heptan-7-one ≥98%
VE:
1 * 100 mg
Artikel-Nr:
(BOSSBS-7796R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7796R
Lokale Artikelnummer::
BOSSBS-7796R
Beschreibung:
This gene encodes a kinetochore protein that functions aspart of the minichromosome instability-12 centromere complex. Theencoded protein is required for proper kinetochore assembly andprogression through the cell cycle. Alternative splicing results inmultiple transcript variants. [provided by RefSeq, Feb 2009].
VE:
1 * 100 µl
Artikel-Nr:
(BLDPBD104590-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD104590-100MG
Lokale Artikelnummer::
BLDPBD104590-100MG
Beschreibung:
2-(5-Methoxythiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 95%
VE:
1 * 100 mg
Artikel-Nr:
(BLDPBD28091-1G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD28091-1G
Lokale Artikelnummer::
BLDPBD28091-1G
Beschreibung:
6-Methoxy-3,4-dihydroisoquinolin-1(2H)-one 97%
VE:
1 * 1 g
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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