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2,2\\\',4,5-Tetrachlorbiphenyl+(PCB+Nr.+48)
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2,2\\\',4,5-Tetrachlorbiphenyl+(PCB+Nr.+48)
Lieferant:
Sigma-Aldrich
Beschreibung:
Isopropylisocyanat, Sigma-Aldrich®
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1,6:2,3-Dianhydro-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyl)-β-D-mannopyranose ≥99%
Lieferant:
DWK Life Sciences
Beschreibung:
Jars, made of clear soda-lime glass, straight sided.
Lieferant:
WEPA PUALUS AND THEWALT
Beschreibung:
Runde Weithalsflasche gemäß der hydrolytischen Klasse III.
Lieferant:
Sigma-Aldrich
Beschreibung:
Magnesiumoxid, Sigma-Aldrich®
Artikel-Nr:
(BNUM1152-50)
Lieferant:
Biotium
Hersteller-Artikelnummer::
BNUM1152-50
Lokale Artikelnummer::
BTIUBNUM1152-50
Beschreibung:
This antibody recognizes a 45 kDa protein, which is identified as isocitrate dehydrogenase (IDH1). It belongs to the isocitrate and isopropylmalate dehydrogenases family. IDH1 catalyzes the third step of the citric acid cycle, which involves the oxidative decarboxylation of isocitrate, formingalpha-ketoglutarate and CO2 in a two-step reaction. The first step involves the oxidation of isocitrate to the intermediate oxalosuccinate, while the second step involves the production ofalpha-ketoglutarate. During this process, either NADH or NADPH is produced along with CO2. Recently, an inactivating mutation of IDH1 has been implicated in glioblastoma. IDH1 appears to function as a tumor suppressor that, when mutationally inactivated, contributes to tumorigenesis in part through induction of the HIF-1 pathway.
VE:
1 * 50 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
1-Chlor-2,2-dimethylpropan, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-5773R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5773R-CY7
Lokale Artikelnummer::
BOSSBS-5773R-CY7
Beschreibung:
FGF22 is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The mouse homolog of this gene was found to be preferentially expressed in the inner root sheath of the hair follicle, which suggested a role in hair development.Fibroblast Growth Factor-22 stimulates the proliferation and activation of cells that express FGF receptor.
VE:
1 * 100 µl
Artikel-Nr:
(SEMA3197)
Lieferant:
SEMADENI
Hersteller-Artikelnummer::
3197
Lokale Artikelnummer::
SEMA3197
Beschreibung:
PP, with screw cap.
VE:
1 * 100 ST
Artikel-Nr:
(BOSSBS-12144R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12144R-A555
Lokale Artikelnummer::
BOSSBS-12144R-A555
Beschreibung:
Src homology 2 (SH2) domains bind specifically to tyrosine-phosphorylated proteins that temporally participate in signal transduction events (1). Shc-like protein (Sck) is a neuronal adaptor protein that contains an N-terminal PTB (phosphotyrosine binding) domain, a collagen homology (CH) domain, and a conserved C-terminal SH2 domain (2,3). Human Sck transcripts are present at high levels in liver, pancreas, prostate and ovary (4,5). In vascular endothelial cells, Sck participates in VEGF-induced signal transduction (6). Treatment of human umbilical vein endothelial (HUVEC) cells with VEGF induces recruitment of Sck to tyrosine-1175 of the kinase insert domain-containing receptor (KDR) and enhances Sck tyrosine phosphorylation (7,8).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12144R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12144R-A647
Lokale Artikelnummer::
BOSSBS-12144R-A647
Beschreibung:
Src homology 2 (SH2) domains bind specifically to tyrosine-phosphorylated proteins that temporally participate in signal transduction events (1). Shc-like protein (Sck) is a neuronal adaptor protein that contains an N-terminal PTB (phosphotyrosine binding) domain, a collagen homology (CH) domain, and a conserved C-terminal SH2 domain (2,3). Human Sck transcripts are present at high levels in liver, pancreas, prostate and ovary (4,5). In vascular endothelial cells, Sck participates in VEGF-induced signal transduction (6). Treatment of human umbilical vein endothelial (HUVEC) cells with VEGF induces recruitment of Sck to tyrosine-1175 of the kinase insert domain-containing receptor (KDR) and enhances Sck tyrosine phosphorylation (7,8).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9716R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9716R-A555
Lokale Artikelnummer::
BOSSBS-9716R-A555
Beschreibung:
Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9716R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9716R-A488
Lokale Artikelnummer::
BOSSBS-9716R-A488
Beschreibung:
Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8389R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8389R-CY7
Lokale Artikelnummer::
BOSSBS-8389R-CY7
Beschreibung:
Essential component of the SCF (SKP1-CUL1-F-box protein) ubiquitin ligase complex, which mediates the ubiquitination of proteins involved in cell cycle progression, signal transduction and transcription. In the SCF complex, serves as an adapter that links the F-box protein to CUL1. SCF(BTRC) mediates the ubiquitination of NFKBIA at 'Lys-21' and 'Lys-22'; the degradation frees the associated NFKB1-RELA dimer to translocate into the nucleus and to activate transcription. SCF(Cyclin F) directs ubiquitination of CP110.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8389R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8389R-CY5
Lokale Artikelnummer::
BOSSBS-8389R-CY5
Beschreibung:
Essential component of the SCF (SKP1-CUL1-F-box protein) ubiquitin ligase complex, which mediates the ubiquitination of proteins involved in cell cycle progression, signal transduction and transcription. In the SCF complex, serves as an adapter that links the F-box protein to CUL1. SCF(BTRC) mediates the ubiquitination of NFKBIA at 'Lys-21' and 'Lys-22'; the degradation frees the associated NFKB1-RELA dimer to translocate into the nucleus and to activate transcription. SCF(Cyclin F) directs ubiquitination of CP110.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11340R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11340R-CY7
Lokale Artikelnummer::
BOSSBS-11340R-CY7
Beschreibung:
The regulated translation of messenger RNA is essential for cell-cycle progression, establishment of the body plan during early development and modulation of key activities in the central nervous system. Cytoplasmic polyadenylation, one mechanism of controlling translation, is driven by cytoplasmic polyadenylation element binding proteins, called CPEBs. CPEB3 (cytoplasmic polyadenylation element binding protein 3) is a 698 amino acid protein that contains two RNA recognition motif (RRM) domains and, like other CPEB proteins, may play a role in the maturation of the central nervous system. CPEB3 exists as multiple alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome.
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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