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1,2-Bis(diphenylphosphino)ethan
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Practically free of homologs.
Artikel-Nr:
(BOSSBS-11698R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-A555
Lokale Artikelnummer::
BOSSBS-11698R-A555
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:
(BOSSBS-11698R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-A680
Lokale Artikelnummer::
BOSSBS-11698R-A680
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 1100 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:
(BOSSBS-11698R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11698R-FITC
Lokale Artikelnummer::
BOSSBS-11698R-FITC
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:
(BOSSBS-11003R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11003R-A680
Lokale Artikelnummer::
BOSSBS-11003R-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 FAM62A gene product has been provisionally designated FAM62A pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8229R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8229R-A680
Lokale Artikelnummer::
BOSSBS-8229R-A680
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 characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(APOSOR1158-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR1158-25G
Lokale Artikelnummer::
APOSOR1158-25G
Beschreibung:
α-Naphthoflavon
VE:
1 * 25 g
Lieferant:
VWR Collection
Beschreibung:
Dieses Zwei-in-Eins-Laborwassersystem stellt aus Leitungswasser Reinst- (Typ I) und RO-Wasser (Typ III) her. Die Qualität des Reinstwassers erfüllt oder übertrifft ASTM-, CLSI-, CAP-, und ISO-Typ-I-Wasserstandards.
Artikel-Nr:
(BOSSBS-3842R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-3842R-CY5
Lokale Artikelnummer::
BOSSBS-3842R-CY5
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
Artikel-Nr:
(BOSSBS-11451R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11451R-CY5
Lokale Artikelnummer::
BOSSBS-11451R-CY5
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-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9448R-CY3
Lokale Artikelnummer::
BOSSBS-9448R-CY3
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:
(1.05242.0250)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.05242.0250
Lokale Artikelnummer::
MERC1.05242.0250
Beschreibung:
Im Allgemeinen bestehen Ionenaustauscher aus einer quervernetzten Polymermatrix mit einer gleichmäßigen Verteilung fester Ionenansammlungen über die Harzstruktur hinweg. Diese müssen durch eine äquivalente Anzahl von Ionen mit entgegengesetzter Ladung, den Gegenionen, im Gleichgewicht gehalten werden, um die elektrische Neutralität zu erhalten. Kationenaustauscher können daher nur Kationen austauschen und anreichern, Anionenaustauscher nur Anionen. Adsorberharze besitzen im Gegensatz dazu einen nicht-ionischen, jedoch je nach Aufbau mehr oder weniger polaren Charakter und adsorbieren nichtstöchiometrisch Anionen, Kationen als auch ungeladene Verbindungen.
VE:
1 * 250 mL
Artikel-Nr:
(APOSPC0259-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC0259-1G
Lokale Artikelnummer::
APOSPC0259-1G
Beschreibung:
2,3-Difluor-p-kresol
VE:
1 * 1 g
Artikel-Nr:
(APOSPC32477-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC32477-1G
Lokale Artikelnummer::
APOSPC32477-1G
Beschreibung:
2'-Fluorbiphenyl-4-carbonsäure
VE:
1 * 1 g
Lieferant:
FLUOROCHEM
Beschreibung:
5-Iod-α,α,α,α',α',α'-Hexafluor-m-xylol
Artikel-Nr:
(SCTV399202)
Lieferant:
S.C.A.T.
Hersteller-Artikelnummer::
399202
Lokale Artikelnummer::
SCTV399202
Beschreibung:
Die Starter-Kits bestehend aus SCAT SafetyCaps, Blindstopfen, Fittings und Luftventilen für die Versorgung von HPLC-Anlagen.
VE:
1 * 1 ST
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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