2,4-Bis(trifluoromethyl)pyridine
Artikel-Nr:
(HONE11176.9030)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
11176.9030
Lokale Artikelnummer::
HONE11176.9030
Beschreibung:
Antimon(III)oxid
VE:
1 * 30 kg
Lieferant:
Honeywell Chemicals
Beschreibung:
Eisen(III)sulfat Hydrat 21-23% (Fe-Basis), Puriss. p.a., Fluka™
Artikel-Nr:
(USBI146405)
Lieferant:
US Biological
Hersteller-Artikelnummer::
146405
Lokale Artikelnummer::
USBI146405
Beschreibung:
Anti-LRFN5 Rabbit Polyclonal Antibody
VE:
1 * 100 µG
Artikel-Nr:
(SIAL309281-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
309281-100G
Lokale Artikelnummer::
SIAL309281-100G
Beschreibung:
Used as chemical actinometer based on photolysis of ferrioxalate in presence of polyoxometalate in aqueous solution.
VE:
1 * 100 g
Lieferant:
Sigma-Aldrich
Beschreibung:
Eisen(III)-nitrat Nonahydrat, Sigma-Aldrich®
Lieferant:
Bernd Kraft
Beschreibung:
Eisen(III)-nitrat Nonahydrat analytisches Reagens
Lieferant:
Alfa Aesar
Beschreibung:
Chrom(III)kaliumsulfat Dodecahydrat ≥99,9% (Metall-Basis)
Artikel-Nr:
(BOSSBS-11637R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11637R-A680
Lokale Artikelnummer::
BOSSBS-11637R-A680
Beschreibung:
Fe65L2 is a 486 amino acid protein that contains one WW domain and two PID domains. Binding to the intracellular domain of the -Amyloid precursor protein, Fe65L2 is thought to modulate the internalisation and, therefore, the accessibility and function of -Amyloid. Via its ability to control the intracellular accumulation of -Amyloid, Fe65L2 is thought to play a role in the pathogenesis of Alzheimer's disease. Fe65L2 exists as four alternatively spliced isoforms designated isoform I, isoform II, isoform III and isoform IV. Fe65L2 interacts with Amyloid-like protein and is encoded by a gene located on human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukaemias and myelodysplastic syndrome.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Rhodium(III)chlorid Hydrat, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-1383R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1383R-CY5.5
Lokale Artikelnummer::
BOSSBS-1383R-CY5.5
Beschreibung:
Broad specificity aminopeptidase. Plays a role in the final digestion of peptides generated from hydrolysis of proteins by gastric and pancreatic proteases. May play a critical role in the pathogenesis of cholesterol gallstone disease. May be involved in the metabolism of regulatory peptides of diverse cell types, responsible for the processing of peptide hormones, such as angiotensin III and IV, neuropeptides, and chemokines. Found to cleave antigen peptides bound to major histocompatibility complex class II molecules of presenting cells and to degrade neurotransmitters at synaptic junctions. Is also implicated as a regulator of IL-8 bioavailability in the endometrium, and therefore may contribute to the regulation of angiogenesis. Is used as a marker for acute myeloid leukemia and plays a role in tumor invasion. In case of human coronavirus 229E (HCoV-229E) infection, serves as receptor for HCoV-229E spike glycoprotein. Mediates as well human cytomegalovirus (HCMV) infection.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9199R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9199R
Lokale Artikelnummer::
BOSSBS-9199R
Beschreibung:
Ig (immunoglobulin) superfamily members exhibit functional characteristics including immune responses, growth factor signaling and cell adhesion. IGSF9 (immunoglobulin superfamily, member 9), also known as Nrt1 or IGSF9A, is a 1,179 amino acid single-pass type I membrane protein expressed in a wide variety of fetal tissues at eight and fourteen weeks of gestation. Belonging to the immunoglobulin superfamily and the Turtle family, IGSF9 is thought to play a role in dendrite outgrowth and synapse maturation. IGSF9 contains two fibronectin type-III domains and five Ig-like (immunoglobulin-like) domains. IGSF9 interacts with MAGI-2 and Shank 1, both of which contain SH3 (Src-homology 3) domains. Protein-protein interactions are central events in cellular signal transduction and are often mediated by SH3 domains. IGSF9 is encoded by a gene located on human chromosome 1q23.2 and mouse chromosome 1 H3.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12361R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12361R-A750
Lokale Artikelnummer::
BOSSBS-12361R-A750
Beschreibung:
The leucine-rich (LRR) repeat is a 20 to 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. FLRT1 (fibronectin leucine rich transmembrane protein 1) is a 646 amino acid single-pass type I membrane protein that contains one fibronectin type-III domain and ten LRR repeats. Expressed in kidney and brain, FLRT1 is thought to play a role in cell adhesion and receptor Signalling. FLRT1 shares similarity with FLRT2 and FLRT3 and is subject to post-translational N-glycosylation. The gene encoding FLRT1 maps to human chromosome 11, which houses over 1400 genes and comprises nearly 4% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11637R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11637R-A555
Lokale Artikelnummer::
BOSSBS-11637R-A555
Beschreibung:
Fe65L2 is a 486 amino acid protein that contains one WW domain and two PID domains. Binding to the intracellular domain of the ∫-Amyloid precursor protein, Fe65L2 is thought to modulate the internalization and, therefore, the accessibility and function of ∫-Amyloid. Via its ability to control the intracellular accumulation of ∫-Amyloid, Fe65L2 is thought to play a role in the pathogenesis of Alzheimer's disease. Fe65L2 exists as four alternatively spliced isoforms designated isoform I, isoform II, isoform III and isoform IV. Fe65L2 interacts with Amyloid-like protein and is encoded by a gene located on human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12361R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12361R-CY3
Lokale Artikelnummer::
BOSSBS-12361R-CY3
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. FLRT1 (fibronectin leucine rich transmembrane protein 1) is a 646 amino acid single-pass type I membrane protein that contains one fibronectin type-III domain and ten LRR repeats. Expressed in kidney and brain, FLRT1 is thought to play a role in cell adhesion and receptor signaling. FLRT1 shares similarity with FLRT2 and FLRT3 and is subject to post-translational N-glycosylation. The gene encoding FLRT1 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1383R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1383R-A750
Lokale Artikelnummer::
BOSSBS-1383R-A750
Beschreibung:
Broad specificity aminopeptidase. Plays a role in the final digestion of peptides generated from hydrolysis of proteins by gastric and pancreatic proteases. May play a critical role in the pathogenesis of cholesterol gallstone disease. May be involved in the metabolism of regulatory peptides of diverse cell types, responsible for the processing of peptide hormones, such as angiotensin III and IV, neuropeptides, and chemokines. Found to cleave antigen peptides bound to major histocompatibility complex class II molecules of presenting cells and to degrade neurotransmitters at synaptic junctions. Is also implicated as a regulator of IL-8 bioavailability in the endometrium, and therefore may contribute to the regulation of angiogenesis. Is used as a marker for acute myeloid leukemia and plays a role in tumor invasion. In case of human coronavirus 229E (HCoV-229E) infection, serves as receptor for HCoV-229E spike glycoprotein. Mediates as well human cytomegalovirus (HCMV) infection.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-11637R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11637R-A350
Lokale Artikelnummer::
BOSSBS-11637R-A350
Beschreibung:
Fe65L2 is a 486 amino acid protein that contains one WW domain and two PID domains. Binding to the intracellular domain of the ∫-Amyloid precursor protein, Fe65L2 is thought to modulate the internalization and, therefore, the accessibility and function of ∫-Amyloid. Via its ability to control the intracellular accumulation of ∫-Amyloid, Fe65L2 is thought to play a role in the pathogenesis of Alzheimer's disease. Fe65L2 exists as four alternatively spliced isoforms designated isoform I, isoform II, isoform III and isoform IV. Fe65L2 interacts with Amyloid-like protein and is encoded by a gene located on human chromosome 5, which contains 181 million base pairs and comprises nearly 6% of the human genome. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
VE:
1 * 100 µl
Preis auf Anfrage
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