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1,2-Propylendiamin
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1,2-Propylendiamin
Artikel-Nr:
(BOSSBS-5049R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5049R-CY7
Lokale Artikelnummer::
BOSSBS-5049R-CY7
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:
GRANT INSTRUMENTS
Beschreibung:
Qualitativ hochwertige, digitale, statische Wasserbäder mit einer Auswahl an Modellen von 2 bis 34 Litern und einem dualen Bad mit 5 und 12 Liter. Duale Bäder sind ideal, wenn zwei unterschiedliche Temperaturen benötigt werden und der Platz begrenzt ist. Alle Einheiten haben Edelstahltanks und langlebige lackierte Stahlgehäuse, bieten schnelle Aufheizzeiten, eine ausgezeichnete Temperaturkontrolle, benutzerfreundliche Bedienelemente und eine helle, übersichtliche Anzeige. Alle Bäder sind mit Heizmattentechnologie für einen optimalen Arbeitsbereich ausgestattet, und ohne Heizelement im Tank sind sie leichter zu reinigen. Die 12-Liter- und größeren Modelle verfügen über einen praktischen Ablaufhahn an der Vorderseite des Bads. Das Sortiment ist ideal für die universitäre Forschung und Lehre sowie Anwendungen in den Bereichen Pharma/Biotechnologie, Gesundheitswesen und Industrie.
Artikel-Nr:
(BOSSBS-11451R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11451R-A680
Lokale Artikelnummer::
BOSSBS-11451R-A680
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 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-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11451R-A647
Lokale Artikelnummer::
BOSSBS-11451R-A647
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:
(BOSSBS-9448R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-A555
Lokale Artikelnummer::
BOSSBS-9448R-A555
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-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-A680
Lokale Artikelnummer::
BOSSBS-9448R-A680
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
(R)-(-)-sec-Butylamin
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-(tert-Butoxymethyl)phenylboronic acid
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:
ANSELL HEALTH CARE
Beschreibung:
Diese nahtlos gestrickten Träger mit Intercept™-Garn sind mit einer ¾-Tauchbeschichtung, oder Nitril-Vollbeschichtung erhältlich.
Artikel-Nr:
(BOSSBS-9887R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9887R-A680
Lokale Artikelnummer::
BOSSBS-9887R-A680
Beschreibung:
p22HBP, also known as HEBP1 (heme binding protein 1), HBP or HEBP, is a 189 amino acid intracellular tetrapyrrole-binding protein that assists in prevention of cellular toxicity by removing free porphyrinogens from the cell. Existing as a monomer, p22HBP localizes to cytoplasm and contains a 21 amino acid chemoattractant within its N-terminus that functions as a natural ligand for FPR3. p22HBP is a member of the HEBP family and binds N-methylprotoporphyrin and metalloporphyrins with similar affinity to porphyrinogens. The gene encoding p22HBP 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:
(BOSSBS-9743R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9743R-CY5
Lokale Artikelnummer::
BOSSBS-9743R-CY5
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKLE2 (ankyrin repeat and LEM domain containing 2), also known as LEMD7, is a 938 amino acid single-pass membrane protein containing an ANK repeat and a LEM domain. Exsiting as two isoforms produced by alternative splicing events, the gene encoding ANKLE2 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:
(BOSSBS-9743R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9743R
Lokale Artikelnummer::
BOSSBS-9743R
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKLE2 (ankyrin repeat and LEM domain containing 2), also known as LEMD7, is a 938 amino acid single-pass membrane protein containing an ANK repeat and a LEM domain. Exsiting as two isoforms produced by alternative splicing events, the gene encoding ANKLE2 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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Photoinitiator/Photoacid Generator
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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
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