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3-(3-Hydroxy-phenyl)-acrylic+acid+ethyl+ester


149 821  results were found

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Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13280R-FITC
Lokale Artikelnummer:: BOSSBS-13280R-FITC
Beschreibung:   The mammalian c-H-, c-K- and N-Ras proto-oncogenes encode ubiquitously expressed proteins (1,2). p21Ras can exist in either a physiologically quiescent GDP-binding state or a GTP-binding signal-emitting state (3). Oncogenic p21Ras proteins are trapped in the excited signal-emitting state because the mechanism normally employed to delimit their excitation period, hydrolysis of their bound GTP to GDP, is impaired as a result of specific mutations (3). Interaction of p21Ras with GTPase activating protein (GAP) can increase hydrolysis of p21Ras-bound GTP by as much as 1000-fold (4,5). The product of the neurofibromatosis type 1 gene (NF1) has also been shown to exhibit p21Ras GAP activity (6,7), and proteins that stimulate the GTPase activity of three other low molecular weight GTPases, including Rho, Rab 3A and Rap 1, have also been described (8,9).
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-9025R-CY5.5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9025R-CY5.5
Lokale Artikelnummer:: BOSSBS-9025R-CY5.5
Beschreibung:   The leucine-rich (LRR) repeat is a 20-30 amino acid motif that forms a hydrophobic å/∫ horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. ISLR2 (immunoglobulin superfamily containing leucine-rich repeat 2), also known as LINX (leucine-rich repeat domain and immunoglobulin domain-containing axon extension protein), is a 745 amino acid single-pass membrane protein that contains five LRR repeats, one Ig-like (immunoglobulin-like) domain, a LRRCT domain and one LRRNT domain. ISLR2 exists as a homomultimer and is essential for axon extension during neural development. The gene encoding ISLR2 maps to human chromosome 15q24.1.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-9980R-A680
Lokale Artikelnummer:: BOSSBS-9980R-A680
Beschreibung:   The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukaemias. DnaJC28 (DnaJ homolog subfamily C member 28), also known as C21orf55, C21orf78 or MGC27620 is a 388 amino acid protein that is expressed in the fetal and adult brain, testis, uterus, spleen and liver. It has been suggested that DnaJC28 may play a role in protein folding or as a chaperone. The DnaJC28 gene product has been provisionally designated DnaJC28 pending further characterisation.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-13236R-CY5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13236R-CY5
Lokale Artikelnummer:: BOSSBS-13236R-CY5
Beschreibung:   Fyb (Fyn binding protein) and the anchoring proteins SKAP55 (src kinase-associated phosphoprotein) and SKAP55-R (SKAP55-related protein) associate with the tyrosine kinase p59fyn (1–3). SKAP55 and SKAP55-R bind to Fyb through their SH3 domains and function as substrates for p59Fyn in resting T cells (1–3). SKAP55 contains an amino-terminal pleckstrin homology domain and a carboxy-terminal SH3 domain binding motif of adjacent arginine and lysine residues followed by tandem tyrosines (i.e. RKxxYxxY) (4,5). SKAP55-R, similar in overall structure to SKAP55, contains a coiled-coil N-terminal domain (1,2). SKAP55 associates with SLAP-130, another component of the Fyn complex, which plays a role in the regulation of signaling events initiated by lymphocyte antigen receptors leading up to T cell activation (6). The human Fyb gene maps to chromosome 5p13.1 and encodes a 783 amino acid protein (7).
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-6505R-CY7
Lokale Artikelnummer:: BOSSBS-6505R-CY7
Beschreibung:   Lipoxygenases are a family of enzymes which dioxygenate unsaturated fatty acids, thus initiating lipoperoxidation of membranes and synthesis of signaling molecules, as well as inducing structural and metabolic changes in the cell. The Lox enzymes in mammals include 12-LO and 15-LO, which are classified with respect to their positional specificity of the deoxygenation of their most common substrate, arachidonic acid. The metabolism of arachidonic acid leads to the generation of biologically active metabolites that have been implicated in cell growth and proliferation, as well as survival and apoptosis. 15-Lipoxygenase (15-LO) acts in physiological membrane remodeling and the pathogenesis of atherosclerosis, inflammation, and carcinogenesis. It is highly regulated and expressed in a tissue- and cell-type-specific fashion. IL-4 and IL-13 play important roles in transactivating the 15-LO gene. Overexpression of 15-LO type 1 in prostate cancer contributes to the cancer progression by regulating IGF-1R expression and activation.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-12498R-CY3)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-12498R-CY3
Lokale Artikelnummer:: BOSSBS-12498R-CY3
Beschreibung:   Apolipoproteins are protein components of plasma lipoproteins (1). The apolipoprotein L gene family encodes six highly homologous proteins designated apoL-I to -VI, which are associated with large high density type lipoproteins (HDL) (2,3). The human apoL family maps to chromosome 22q12.1-13.1 within a 127,000-bp region (4). ApoL has been characterized as a pancreas specific, 383-amino acid protein that contains a 12-amino acid secretory signal peptide (4). The apoL genes have TATA-less promoters and contain putative sterol regulatory elements, suggesting that transcription of these genes may be coordinated with that of the low density lipoprotein receptor and genes in pathways involving the synthesis of triglycerides and cholesterol (3). ApoL homologs can undergo 10 fold changes in expression during atherosclerotic changes in vascular endothelial cells, which includes the inflammatory reaction of atherosclerotic lesions (5).
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8042R-CY3
Lokale Artikelnummer:: BOSSBS-8042R-CY3
Beschreibung:   The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
VE:  1 * 100 µl
Artikel-Nr: (BOSSBS-8042R-CY5.5)

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-8042R-CY5.5
Lokale Artikelnummer:: BOSSBS-8042R-CY5.5
Beschreibung:   The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-13628R-CY3
Lokale Artikelnummer:: BOSSBS-13628R-CY3
Beschreibung:   The C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily consists of a variety of proteins that share a common protein fold and have diverse functions, including cell-cell signaling, cell adhesion, glycoprotein turnover and immune responses. CLEC-12A (C-type lectin domain family 12, member A), also known as CLL1, MICL, CLL-1 or DCAL-2, is a 275 amino acid single-pass type II membrane protein that contains one C-type lectin domain and belongs to the CTL/CTLD superfamily. Existing as multiple alternatively spliced isoforms that are expressed in neutrophils, eosinophils, monocytes and dendritic cells, CLEC-12A functions as a cell surface receptor that acts as a negative regulator of granulocyte and monocyte function and, via this activity, modulates signaling cascades. CLEC-12A is highly subject to post-translational glycosylation at its N-terminus and may also exist as a homodimer.
VE:  1 * 100 µl

Lieferant:  Bioss
Hersteller-Artikelnummer:: BS-11153R-CY5
Lokale Artikelnummer:: BOSSBS-11153R-CY5
Beschreibung:   Protocadherins are a large family of cadherin-like cell adhesion proteins that are involved in the establishment and maintenance of neuronal connections in the brain. There are three protocadherin gene clusters, designated alpha, beta and gamma, all of which contain multiple tandemly arranged genes. PCDHB12 (Protocadherin beta 12) is a 795 amino acid protein that is one of 16 proteins in the protocadherin beta cluster. Unlike the alpha and gamma gene clusters whose genes are spliced to downstream constant region exons during transcription, members of the beta cluster (such as PCDHB12) do not use constant-region exons to produce mRNAs. As a result, each protocadherin beta gene encodes the transmembrane, extracellular and short cytoplasmic domains of the protein. Localized to the cell membrane, PCDHB12 is a single-pass type I membrane protein that contains six cadherin domains. PCDHB12 may participate in the establishment and maintenance of specific neuronal connections in the brain.
VE:  1 * 100 µl
Lieferant:  KARTELL
Beschreibung:   PP, weiß
Artikel-Nr: (EHERC20505000)

Lieferant:  EHRENSTORFER
Hersteller-Artikelnummer:: C20505000
Lokale Artikelnummer:: EHERC20505000
Beschreibung:   Acenaphthen
VE:  1 * 100 mg
Lieferant:  NICKEL ELECTRO
Hersteller-Artikelnummer:: 6900
Lokale Artikelnummer:: NICK6900
Beschreibung:   Gestelle aus Edelstahl, Für: 12 Reagenzgläser, Ø 30 mm
VE:  1 * 1 ST
Artikel-Nr: (217-0799)

Lieferant:  DWK Life Sciences
Hersteller-Artikelnummer:: 286123809
Lokale Artikelnummer:: SCOT286123809
Beschreibung:   DURAN®, borosilicate glass 3.3, clear.
VE:  1 * 1 ST
Lieferant:  GLOBAL COOLING
Hersteller-Artikelnummer:: ULT25NEU-EU
Lokale Artikelnummer:: GLCLULT25NEU-EU
Beschreibung:   Der ULT25NEU ist die einzige heute verfügbare tragbare ULT-Gefrierschranklösung, mit der die ULT-Lagerung zum Patienten gebracht werden kann. Dieser kleine, leichte und effiziente tragbare Gefrierschrank mit −80 °C ist ideal für klinische Studien und die Verabreichung biologischer Arzneimittel.
VE:  1 * 1 ST
Artikel-Nr: (CARBPTC1220-230SN)

Lieferant:  CARBOLITE
Hersteller-Artikelnummer:: PTC1220-230SN
Lokale Artikelnummer:: CARBPTC1220-230SN
Beschreibung:   Tube Furnace, PTC 12/20/150, Max. Temp.: 1200 °C, Beheizte Länge: 150 mm, Rohr I-Ø: 20 mm, Leistung: Max. 1100 W, Außen B×T×H: 311×229×400 mm
VE:  1 * 1 ST
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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