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3,5-Dioxocyclohexanecarboxylic acid
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3,5-Dioxocyclohexanecarboxylic acid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Active fluoromethylene group, useful reagent for the synthesis of fluoro-heterocycles, e.g Pyrimidines; also can produce fluorinated trisubstituted alkenes, ask for refs.
Artikel-Nr:
(BOSSBS-13319R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13319R-A680
Lokale Artikelnummer::
BOSSBS-13319R-A680
Beschreibung:
Belonging to the glycosyltransferase 14 family, GCNT7, also known as Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 7, is a 430 amino acid glycosyltransferase that is localized to the Golgi apparatus. Other members of this family include GCNT1, GCNT2, GCNT3, GCNT4 and GCNT6. GCNT1 has been shown to play an important regulatory role in the biosynthesis of mucin-type O-glycans, which serve as ligands in cell adhesion. Specifically, GCNT1 expression in leukocytes regulates the synthesis of core 2 O-glycans that carry sialyl-Lewis x (sLex) oligosaccharides, which confer high affinity binding to Selectin proteins. Since downregulation of Selectin ligand expression has been shown to inhibit tissue infiltration, glycosyltransferase 14 family members represent potential drug targets for the treatment of inflammatory disorders and other pathologies involving Selectin proteins.
VE:
1 * 100 µl
Lieferant:
Avantor
Beschreibung:
Tetrahydrofuran ≥99,8% (durch GC, auf Wasserinhalt korrigiert) enthält keine Konservierungsstoffe, BAKER ANALYZED® HPLC für die HPLC, UHPLC, für die Spektrophotometrie, J.T.Baker®
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2H-Perfluoro-5,8,11,14,17-pentamethyl-3,6,9,12,15,18-hexaoxahenicosane 95%
Artikel-Nr:
(USBI029718)
Lieferant:
US Biological
Hersteller-Artikelnummer::
029718
Lokale Artikelnummer::
USBI029718
Beschreibung:
Anti-AMY2B Rabbit Polyclonal Antibody
VE:
1 * 100 µG
Lieferant:
Alfa Aesar
Beschreibung:
Sodium-1-naphthalenesulphonate, (max. 2% H₂O) 99% (Trockengewicht)
Artikel-Nr:
(BOSSBS-8336R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8336R-CY5.5
Lokale Artikelnummer::
BOSSBS-8336R-CY5.5
Beschreibung:
TMEM147, also known as ; NIFIE 14, is a 224 amino acid protein encoded by a gene mapping to human chromosome 19. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
Ethyl-N-(diphenylmethylen)glycinat 98%
Artikel-Nr:
(MOLE25038144-500G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
25038144-500G
Lokale Artikelnummer::
MOLE25038144-500G
Beschreibung:
1,4-Naphthochinon
VE:
1 * 500 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
Alfa Aesar
Beschreibung:
(1,3-Dioxolan-2-ylmethyl)triphenylphosphoniumbromid ≥98%
Artikel-Nr:
(BOSSBS-5025R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5025R
Lokale Artikelnummer::
BOSSBS-5025R
Beschreibung:
The Claudin superfamily consists of many structurally related proteins in humans. These proteins are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Three classes of proteins are known to localize to tight junctions, including the claudins, Occludin and Junction adhesion molecules. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. Claudin expression is often highly restricted to specfic regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-14 is a multi-pass membrane protein that is expressed in liver, kidney and ear. Defects in the gene encoding claudin-14 are the cause of non-syndromic sensorineural deafness autosomal recessive type 29 (DFNB29), a form of hearing loss resulting from damage to either nerve pathways or neural receptors of the inner ear.
VE:
1 * 100 µl
Lieferant:
Merck
Beschreibung:
EMPLURA® is our low-cost alternative to high-purity qualities. With EMPLURA® we offer a range of solvents for a plurality of basic applications in non-regulated industries and for less demanding applications, preparative laboratory work and cleaning purposes. EMPLURA® solvents provide adequate specifications with the most important parameters.
Artikel-Nr:
(BOSSBS-5025R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5025R-HRP
Lokale Artikelnummer::
BOSSBS-5025R-HRP
Beschreibung:
The Claudin superfamily consists of many structurally related proteins in humans. These proteins are important structural and functional components of tight junctions in paracellular transport. Claudins are located in both epithelial and endothelial cells in all tight junction-bearing tissues. Three classes of proteins are known to localize to tight junctions, including the claudins, Occludin and Junction adhesion molecules. Claudins, which consist of four transmembrane domains and two extracellular loops, make up tight junction strands. Claudin expression is often highly restricted to specfic regions of different tissues and may have an important role in transcellular transport through tight junctions. Claudin-14 is a multi-pass membrane protein that is expressed in liver, kidney and ear. Defects in the gene encoding claudin-14 are the cause of non-syndromic sensorineural deafness autosomal recessive type 29 (DFNB29), a form of hearing loss resulting from damage to either nerve pathways or neural receptors of the inner ear.
VE:
1 * 100 µl
Lieferant:
Alfa Aesar
Beschreibung:
1-Boc-isonipecotinsäureethylester ≥97%
Artikel-Nr:
(BOSSBS-2352R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2352R-A750
Lokale Artikelnummer::
BOSSBS-2352R-A750
Beschreibung:
Cytochromes P45 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidises a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Acts as a 1,4-cineole 2-exo-monooxygenase.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11185R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11185R
Lokale Artikelnummer::
BOSSBS-11185R
Beschreibung:
The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. Unlike its related family members, this smallest known acidic cytokeratin is not paired with a basic cytokeratin in epithelial cells. It is specifically expressed in the periderm, the transiently superficial layer that envelopes the developing epidermis. The type I cytokeratins are clustered in a region of chromosome 17q12-q21.<be>This gene encodes the type I intermediate filament chain keratin 17, expressed in nail bed, hair follicle, sebaceous glands, and other epidermal appendages. Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex. [provided by RefSeq, Aug 2008].
VE:
1 * 100 µl
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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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