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Lieferant:
Thermo Scientific
Beschreibung:
Ethylacetoacetat 99+%, reinst
Artikel-Nr:
(1.07026.2500)
Lieferant:
Merck
Hersteller-Artikelnummer::
1.07026.2500
Lokale Artikelnummer::
MERC1.07026.2500
Beschreibung:
Diethylether, EMPARTA® ACS zur Analyse, Supelco®
VE:
1 * 2,5 L
Lieferant:
Alfa Aesar
Beschreibung:
(2-Pyridyl)essigsäureethylester ≥98%
Artikel-Nr:
(BLDPBD129460-25G)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD129460-25G
Lokale Artikelnummer::
BLDPBD129460-25G
Beschreibung:
Ethyloxamat 95%
VE:
1 * 25 g
Lieferant:
Thermo Scientific
Beschreibung:
Ethylisobutyrylacetat 95%
Artikel-Nr:
(MACR6777-16)
Lieferant:
MACRON AVANTOR BRAND
Lokale Artikelnummer::
MACR6777-16
Beschreibung:
Ethanol absolut, wasserfrei ≥99,8% (durch GC), AR®, Macron Fine Chemicals™
VE:
1 * 2,5 L
Lieferant:
Alfa Aesar
Beschreibung:
Ethylpentafluorbenzoat ≥98%
Lieferant:
Alfa Aesar
Beschreibung:
Ethyltridecanoat ≥97%
Lieferant:
Merck
Beschreibung:
Highest purity solvents for UHPLC-MS analysis.
Artikel-Nr:
(BOSSBS-11349R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11349R-HRP
Lokale Artikelnummer::
BOSSBS-11349R-HRP
Beschreibung:
Carbonic anhydrases (CAs), also designated carbonate dehydratases or carbonate hydrolyases, form a large family of genes that encode zinc metalloenzymes of great physiologic importance. As catalysts of the reversible hydration of carbon dioxide, these enzymes participate in a variety of biologic processes, including respiration, acid-base balance, bone resorption and calcification as well as the formation of aqueous humor, cerebrospinal fluid, saliva and gastric acid. Genes in the ?carbonic anhydrase family encode either active carbonic anhydrase isozymes or æ³catalytic?(devoid of CO2 hydration activity) carbonic anhydrase-related proteins. Human CA I (CA1) is encoded by the CA1 gene, which maps to a region on chromosome 8 that harbors a cluster of CA genes. CA I localizes to the cytoplasm and research indicates that a severe deficiency of CA I does not result in any obvious hematological or renal consequences.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1021R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1021R-A680
Lokale Artikelnummer::
BOSSBS-1021R-A680
Beschreibung:
Cooperates with LY96 and CD14 to mediate the innate immune response to bacterial lipopolysaccharide (LPS). Acts via MYD88, TIRAP and TRAF6, leading to NF-kappa-B activation, cytokine secretion and the inflammatory response. Also involved in LPS-independent inflammatory responses triggered by free fatty acids, such as palmitate. In complex with TLR6, promotes sterile inflammation in monocytes/macrophages in response to oxidised low-density lipoprotein (oxLDL) or amyloid-beta 42. In this context, the initial signal is provided by oxLDL- or amyloid-beta 42-binding to CD36. This event induces the formation of a heterodimer of TLR4 and TLR6, which is rapidly internalized and triggers inflammatory response, leading to the NF-kappa-B-dependent production of CXCL1, CXCL2 and CCL9 cytokines, via MYD88 signaling pathway, and CCL5 cytokine, via TICAM1 signaling pathway, as well as IL1B secretion.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12949R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12949R-FITC
Lokale Artikelnummer::
BOSSBS-12949R-FITC
Beschreibung:
CRTAP is a secreted protein localizing to the extracellular space that plays a role in collagen post-translational modifications, extracellular fibril assembly and intracellular trafficking. CRTAP is widely expressed with predominant expression in articular chondrocytes. It contains a signal peptide and a tetratricopeptide-like helical domain and is essential for normal bone formation. In the endoplasmic reticulum (ER), CRTAP forms a complex with Gros1 and CyPB (cyclophilin B) and is required for the efficient 3-hydroxylation of target prolyl residues in Collagen Type I molecules, the major structural proteins of skin and bone. Mutations in the gene encoding CRTAP can lead to autosomal recessive osteogenesis imperfecta (OI) type 7 and type 2B. OI, also known as brittle bone disease, is characterized by bone fragility and susceptibility to fractures. OI type 7 is a mild form of this disorder, while OI type 2B is a neonatal lethal condition.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13059R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13059R-A680
Lokale Artikelnummer::
BOSSBS-13059R-A680
Beschreibung:
Fibulin proteins contribute to normal development of elastic fiber systems in various types of organs that require elasticity, such as vasculature, lung and skin. Fibulin-4, also known as EFEMP2 (EGF-containing fibulin-like extracellular matrix protein 2), MBP1 or UPH1 is a 443 amino acid secreted protein that contains six EGF-like calcium-binding domains and belongs to the fibulin family. Expressed ubiquitously with highest expression in heart, Fibulin-4 is essential for connective tissue development and elastic fiber formation, and may also play an important role in vascular patterning and collagen biosynthesis. Defects in the gene encoding Fibulin-4 are associated with autosomal recessive cutis laxa type I (CL type I), a connective tissue disorder that is inherited in both an autosomal dominant and an autosomal recessive manner and is characterized by inelastic tissue in all affected areas of the body.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9986R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9986R-A750
Lokale Artikelnummer::
BOSSBS-9986R-A750
Beschreibung:
C22orf36 is a 315 amino acid protein that contains two LRR (leucine-rich) repeats and exists as two alternatively spliced isoforms. C22orf36 is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chromosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukaemia.
VE:
1 * 100 µl
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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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