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(\u00B1)-1,2-Pentandiol
Lieferant:
Alfa Aesar
Beschreibung:
5,5-Dimethyl-1,3-dioxan-2-one, tech.
Artikel-Nr:
(B20921.06)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
B20921.06
Lokale Artikelnummer::
ALFAB20921.06
Beschreibung:
5-(2,3-Dichlorphenyl)-1H-tetrazol 97
VE:
1 * 5 g
Lieferant:
Alfa Aesar
Beschreibung:
1,5-Diazobicyclo[4.3.0]-5-nonen ≥98%
Artikel-Nr:
(BOSSBS-11398R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11398R-A750
Lokale Artikelnummer::
BOSSBS-11398R-A750
Beschreibung:
This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. Studies of the orthologous gene in rat have shown that the encoded protein selectively modulates spontaneous synaptic-vesicle exocytosis and may also be involved in regulating calcium independent secretion in nonneuronal cells. Alternative splicing results in multiple transcript variants. The gene has previously been referred to as synaptotagmin XI but has been renamed synaptotagmin XII to be standard with mouse and rat official nomenclature.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5049R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R-CY5.5
Lokale Artikelnummer::
BOSSBS-5049R-CY5.5
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:
IPI-549 is a selective phosphoinositide-3-kinase (PI3K)-γ inhibitor with IC50 of 16 nM as an immuno-oncology clinical candidate.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
N-[Bis(methylsulphanyl)methylidene]-4-chlorobenzene-1-sulphonamide
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
(S)-1-(2-Fluoro-4-methoxyphenyl)ethylamine hydrochloride
Artikel-Nr:
(BLDPBD238951-100MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD238951-100MG
Lokale Artikelnummer::
BLDPBD238951-100MG
Beschreibung:
(S)-2-Azabicyclo[2.2.2]octane-3-carboxylic acid 98%
VE:
1 * 100 mg
Artikel-Nr:
(BOSSBS-9951R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9951R-A680
Lokale Artikelnummer::
BOSSBS-9951R-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 C12orf53 gene product has been provisionally designated C12orf53 pending further characterisation.
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-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-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
Artikel-Nr:
(87888.180)
Lieferant:
VWR Chemicals
Lokale Artikelnummer::
VWRC87888.180
Beschreibung:
Phenolrot Natriumsalz 0,1% in Ethanol 20% Reag. Ph. Eur. 1063601
VE:
1 * 100 mL
Artikel-Nr:
(BOSSBS-3842R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3842R
Lokale Artikelnummer::
BOSSBS-3842R
Beschreibung:
EIF3S3 binds to the 40S ribosome and promotes the binding of methionyl-tRNAi and mRNA. It associates with the p170 subunit of EIF3. The EIF3 is composed of at least 12 different subunits.
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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