Potassium+hexacyanocobaltate(III)
Artikel-Nr:
(BOSSBS-10127R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10127R-A750
Lokale Artikelnummer::
BOSSBS-10127R-A750
Beschreibung:
Required for TCR (T-cell antigen receptor)- and pre-TCR-mediated Signalling, both in mature T-cells and during their development. Involved in FCGR3 (low affinity immunoglobulin gamma Fc region receptor III)-mediated Signalling in natural killer cells and FCER1 (high affinity immunoglobulin epsilon receptor)-mediated Signalling in mast cells. Couples activation of these receptors and their associated kinases with distal intracellular events such as mobilization of intracellular calcium stores, PKC activation, MAPK activation or cytoskeletal reorganization through the recruitment of PLCG1, GRB2, GRAP2, and other Signalling molecules.
VE:
1 * 100 µl
Lieferant:
Biotium
Beschreibung:
CD309, also known as VEGF-R2, KDR3, and Flk-1 (mouse), is a type I transmembrane glycoprotein. It is a member of the CSF-1/PDGF receptor family of type III tyrosine kinase receptors. Human VEGF-R2 is mainly expressed by endothelial cells, embryonic tissues, and megakaryocytes. It plays an important role in the regulation of angiogenesis, vasculogenesis, and vascular permeability. The ligands of VEGF-R2 include VEGF-A, VEGF-C, VEGF-D, and VEGF splice isoforms. Ligation of VEGF-R2 with its ligands results in the receptor dimerization and auto-phosphorylation, stimulating endothelial cell proliferation and migration.
Artikel-Nr:
(BOSSBS-10451R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10451R-A647
Lokale Artikelnummer::
BOSSBS-10451R-A647
Beschreibung:
This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7555R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7555R-A555
Lokale Artikelnummer::
BOSSBS-7555R-A555
Beschreibung:
EphA3 is a member of the Ephrin (Eph) family. The Ephrins and Eph-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the Ephrin A (EphA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the Ephrin B (EphB) class, which are transmembrane proteins. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9054R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9054R-HRP
Lokale Artikelnummer::
BOSSBS-9054R-HRP
Beschreibung:
DOM3Z, also known as NG6 or DOM3L, is a 396 amino acid ubiquitously expressed protein belonging to the Dom3Z family. The gene encoding DOM3Z maps to human chromosome 6 in the major histocompatibility complex (MHC) class III region. Chromosome 6 contains 170 million base pairs and comprises nearly 6% of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease and Stickler syndrome are all associated with genes that map to chromosome 6.
VE:
1 * 100 µl
Lieferant:
FLUOROCHEM
Beschreibung:
Mangan(III)fluorid
Artikel-Nr:
(MOLE43449981-25G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
43449981-25G
Lokale Artikelnummer::
MOLE43449981-25G
Beschreibung:
Sudan III
VE:
1 * 25 g
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Lieferant:
Bernd Kraft
Beschreibung:
Kaliumpermanganat 20 g/l in wässriger Lösung für die Bestimmung von Quecksilber
Artikel-Nr:
(REGE3004200)
Lieferant:
REAGECON
Hersteller-Artikelnummer::
3004200
Lokale Artikelnummer::
REGE3004200
Beschreibung:
Kaliumbromat Reag. Ph. Eur. 3004200
VE:
1 * 1 L
Artikel-Nr:
(FLUO009409-5G)
Lieferant:
FLUOROCHEM
Hersteller-Artikelnummer::
009409-5G
Lokale Artikelnummer::
FLUO009409-5G
Beschreibung:
Ytterbium(III)trifluormethansulfonat
VE:
1 * 5 g
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Lieferant:
Sigma-Aldrich
Beschreibung:
Phosphor(III)bromid, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-10451R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-10451R-CY5
Lokale Artikelnummer::
BOSSBS-10451R-CY5
Beschreibung:
This intronless gene encodes a 70kDa heat shock protein which is a member of the heat shock protein 70 family. In conjuction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. It is also involved in the ubiquitin-proteasome pathway through interaction with the AU-rich element RNA-binding protein 1. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which encode similar proteins. [provided by RefSeq, Jul 2008].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8498R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8498R
Lokale Artikelnummer::
BOSSBS-8498R
Beschreibung:
REG1 beta is a type I subclass member of the Reg gene family. The Reg gene family is a multigene family grouped into four subclasses, types I, II, III and IV based on the primary structures of the encoded proteins. REG1 beta highly similar to the REG1 alpha protein. The related REG1 alpha protein is associated with islet cell regeneration and diabetogenesis, and may be involved in pancreatic lithogenesis. Reg family members REG1 alpha, REGL, PAP and this gene are tandomly clustered on chromosome 2p12 and may have arisen from the same ancestral gene by gene duplication.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7555R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7555R-CY7
Lokale Artikelnummer::
BOSSBS-7555R-CY7
Beschreibung:
EphA3 is a member of the Ephrin (Eph) family. The Ephrins and Eph-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the Ephrin A (EphA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the Ephrin B (EphB) class, which are transmembrane proteins. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7555R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7555R
Lokale Artikelnummer::
BOSSBS-7555R
Beschreibung:
EphA3 is a member of the Ephrin (Eph) family. The Ephrins and Eph-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, especially in the nervous system and in erythropoiesis. Based on their structures and sequence relationships, ephrins are divided into the Ephrin A (EphA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the Ephrin B (EphB) class, which are transmembrane proteins. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-7974R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7974R-CY7
Lokale Artikelnummer::
BOSSBS-7974R-CY7
Beschreibung:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms.
VE:
1 * 100 µl
Preis auf Anfrage
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