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Dimethyl+cubane-1,4-dicarboxylate
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Dimethyl+cubane-1,4-dicarboxylate
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-(tert-Butoxymethyl)phenylboronic acid
Artikel-Nr:
(ANSE11-561/12)
Lieferant:
ANSELL HEALTH CARE
Hersteller-Artikelnummer::
11-561/12
Lokale Artikelnummer::
ANSE11-561/12
Beschreibung:
Ganztägiger Komfort und Schnittschutz.
VE:
1 * 12 PAAR
Artikel-Nr:
(BOSSBS-5049R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R-A350
Lokale Artikelnummer::
BOSSBS-5049R-A350
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:
(BOSSBS-5049R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R-A647
Lokale Artikelnummer::
BOSSBS-5049R-A647
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:
(BOSSBS-9448R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-A488
Lokale Artikelnummer::
BOSSBS-9448R-A488
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9448R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-A750
Lokale Artikelnummer::
BOSSBS-9448R-A750
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1100 genes and comprises approximately 4,5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11451R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11451R-HRP
Lokale Artikelnummer::
BOSSBS-11451R-HRP
Beschreibung:
Advillin is an 819 amino acid protein that localizes to both the cytoplasm and the cytoskeleton and contains one HP domain and six gelsolin-like repeats. Expressed at high levels in colon and small intestine and at lower levels in uterus, thymus, testis and prostate, advillin functions as a calcium-regulated Actin-binding protein that may be involved in the development of neuronal cells, specifically those that form ganglia. The gene encoding advillin maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR370090-250MG)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR370090-250MG
Lokale Artikelnummer::
APOSOR370090-250MG
Beschreibung:
2,3,6,7-Tetrahydro-1H-azepine hydrochloride ≥98%
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Chlor-4,5-diaminobenzotrifluorid 98%
Artikel-Nr:
(APOSOR918460-5G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR918460-5G
Lokale Artikelnummer::
APOSOR918460-5G
Beschreibung:
2-(2,3-Dichlorphenyl)ethanol 96%
VE:
1 * 5 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
tert-Butyl-4-brom-2-fluorbenzoat 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Chloro-3-trifluoromethyl-5-(methyl)pyrazole 97%
Artikel-Nr:
(APOSPC510175-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC510175-1G
Lokale Artikelnummer::
APOSPC510175-1G
Beschreibung:
Ethyl 2,2-Difluoro-3-(methylamino)propanoate hydrochloride
VE:
1 * 1 g
Lieferant:
ENTEGRIS
Beschreibung:
These cartridge filters provide small particle retention to ensure minimal particles remain on the water surface. High purity connections with no O-ring to avoid potential source of contamination ensuring downstream cleanliness.
Artikel-Nr:
(APOSOR345568-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR345568-25G
Lokale Artikelnummer::
APOSOR345568-25G
Beschreibung:
8-Chloro-11-[(n-methyl)-4-piperidylidene]-6,11-dihydro-5h-benzo [5,6] cyclohepta[1,2b]pyridine 97%
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-9448R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-CY5.5
Lokale Artikelnummer::
BOSSBS-9448R-CY5.5
Beschreibung:
The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
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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