Wenn Sie das Fenster schließen, wird Ihre Konfiguration nicht gespeichert, es sei denn, Sie haben Ihren Artikel in die Bestellung aufgenommen oder zu Ihren Favoriten hinzugefügt.
Klicken Sie auf OK, um das MILLIPLEX® MAP-Tool zu schließen oder auf Abbrechen, um zu Ihrer Auswahl zurückzukehren.
Wählen Sie konfigurierbare Panels & Premixed-Kits - ODER - Kits für die zelluläre Signaltransduktion & MAPmates™
Konfigurieren Sie Ihre MILLIPLEX® MAP-Kits und lassen sich den Preis anzeigen.
Konfigurierbare Panels & Premixed-Kits
Unser breites Angebot enthält Multiplex-Panels, für die Sie die Analyten auswählen können, die am besten für Ihre Anwendung geeignet sind. Unter einem separaten Register können Sie das Premixed-Cytokin-Format oder ein Singleplex-Kit wählen.
Kits für die zelluläre Signaltransduktion & MAPmates™
Wählen Sie gebrauchsfertige Kits zur Erforschung gesamter Signalwege oder Prozesse. Oder konfigurieren Sie Ihre eigenen Kits mit Singleplex MAPmates™.
Die folgenden MAPmates™ sollten nicht zusammen analysiert werden: -MAPmates™, die einen unterschiedlichen Assaypuffer erfordern. -Phosphospezifische und MAPmate™ Gesamtkombinationen wie Gesamt-GSK3β und Gesamt-GSK3β (Ser 9). -PanTyr und locusspezifische MAPmates™, z.B. Phospho-EGF-Rezeptor und Phospho-STAT1 (Tyr701). -Mehr als 1 Phospho-MAPmate™ für ein einziges Target (Akt, STAT3). -GAPDH und β-Tubulin können nicht mit Kits oder MAPmates™, die panTyr enthalten, analysiert werden.
.
Bestellnummer
Bestellinformationen
St./Pkg.
Liste
Dieser Artikel wurde zu Ihren Favoriten hinzugefügt.
Wählen Sie bitte Spezies, Panelart, Kit oder Probenart
Um Ihr MILLIPLEX® MAP-Kit zu konfigurieren, wählen Sie zunächst eine Spezies, eine Panelart und/oder ein Kit.
Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
Catalogue Number
Ordering Description
Qty/Pack
List
Dieser Artikel wurde zu Ihren Favoriten hinzugefügt.
Spezies
Panelart
Gewähltes Kit
Menge
Bestellnummer
Bestellinformationen
St./Pkg.
Listenpreis
96-Well Plate
Menge
Bestellnummer
Bestellinformationen
St./Pkg.
Listenpreis
Weitere Reagenzien hinzufügen (MAPmates erfordern die Verwendung eines Puffer- und Detektionskits)
Menge
Bestellnummer
Bestellinformationen
St./Pkg.
Listenpreis
48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
Platzsparende Option Kunden, die mehrere Kits kaufen, können ihre Multiplex-Assaykomponenten in Kunststoffbeuteln anstelle von Packungen erhalten, um eine kompaktere Lagerung zu ermöglichen.
Dieser Artikel wurde zu Ihren Favoriten hinzugefügt.
Das Produkt wurde in Ihre Bestellung aufgenommen
Sie können nun ein weiteres Kit konfigurieren, ein Premixed-Kit wählen, zur Kasse gehen oder das Bestell-Tool schließen.
Detect phospho-TrkA (Tyr794) using this Anti-phospho-TrkA (Tyr794) Antibody validated for use in Western Blotting and Immunocytochemistry.
More>>Detect phospho-TrkA (Tyr794) using this Anti-phospho-TrkA (Tyr794) Antibody validated for use in Western Blotting and Immunocytochemistry. Less<<
Anti-phospho-TrkA (Tyr794) Antibody: SDB (Sicherheitsdatenblätter), Analysenzertifikate und Qualitätszertifikate, Dossiers, Broschüren und andere verfügbare Dokumente.
High affinity nerve growth factor receptor (EC 2.7.10.1; UniProt P35739; also known as Neurotrophic tyrosine kinase receptor type 1, p140-TrkA, Slow nerve growth factor receptor, Trk-A, TrkA neurotrophin receptor, TrkA proto-oncogene receptor, Tropomyosin-related kinase A) is encoded by the Ntrk1 gene (also known as Trk, Trka) in rat (Gene ID 59109). Neurotrophins mediate a wide range of neuronal functions, including survival, differentiation, growth, and death, via two classes of transmembrane receptors, the Trk receptor tyrosine kinase and the p75 neurotrophin receptor. While nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), and NT-4 all bind the p75 receptor, TrkA is selective for NGF, TrkB is selective for BDNF and NT-4, and TrkC is selective for NT-3. TrkA and TrkB receptors can also be activated by ligands of the G-protein-coupled receptor (GPCRs), including the nucleoside adenosine or adenosine agonists, such as CGS 21680 and the pituitary adenylate cyclase-activating polypeptide (PACAP). In addition to transactivation via GPCRs, Glucocorticoids (GCs) are also reported to promote TrkA/B/C activation due to signaling cross-talk between Trk and GC receptor (GR).
References
Product Information
Format
Affinity Purified
Presentation
Purified rabbit polyclonal antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Detect phospho-TrkA (Tyr794) using this Anti-phospho-TrkA (Tyr794) Antibody validated for use in Western Blotting and Immunocytochemistry.
Key Applications
Western Blotting
Immunocytochemistry
Application Notes
Western Blotting Analysis: A representative lot detected NGF-stimulated Tyr794 phosphorylation of exogenously expressed human TrkA in PC12 cells (Courtesy of Dr. Moses V. Chao, Langone Medical Center, New York University). Immunocytochemistry Analysis: A representative lot detected PACAP-induced TrkA Tyr794 phosphorylation in cultured rat basal forebrain neurons (Courtesy of Dr. Moses V. Chao, Langone Medical Center, New York University). Western Blotting Analysis: A representative lot detected NGF-stimulated Tyr794 phosphorylation of exogenously expressed human TrkA in PC12 cells (Rajagopal, R., et al. (2004). 24(30):6650-6658). Western Blotting Analysis: A representative lot detected NGF-stimulated TrkA Tyr794 phosphorylation in cultured rat embryonic E18 septal neurons (Jeanneteau, F., et al. (2008). Proc Natl Acad Sci USA. 105(12):4862-4867). Western Blotting Analysis: A representative lot detected NGF-dependent TrkA Tyr794 phosphorylation in cultured DRG neurons from E16.5 rat embryos (Arevalo, J.C., et al. (2006). Neuron. 50(4):549-559). Immunocytochemistry Analysis: A representative lot detected PACAP38-induced TrkA Tyr794 phosphorylation in cultured rat basal forebrain neurons, as well as CGS 21680- and NGF-induced Tyr794 phosphorylation of exogenously expfressed human TrkA in serum-starved PC12 cultures (Rajagopal, R., et al. (2004). 24(30):6650-6658). Immunocytochemistry Analysis: A representative lot detected NGF-stimulated TrkA Tyr794 phosphorylation in cultured DRG neurons from E16.5 rat embryos (Arevalo, J.C., et al. (2006). Neuron. 50(4):549-559).
Biological Information
Immunogen
Linear peptide corresponding to rat TrkA sequence near the C-terminus with phosphorylated Tyr794.
Epitope
Near C-terminus
Concentration
Please refer to lot specific datasheet.
Host
Rabbit
Specificity
This polyclonal antibody selectively detects NGF-induced pTyr794 phosphorylation of TrkA in cultured primary embryonic rat septal neurons, but not BDNF-induced pTyr816 phosphorylation of TrkB in rat hippocampal neurons (PMID 18347336).
Species Reactivity
Rat
Human
Species Reactivity Note
Rat, Human. Predicted to react with Mouse based on 100% sequence homology.
Evaluated by Western Blotting in NGF treated human TrkA-transfected PC12 cell lysate.
Western Blotting Analysis: 2.0 µg/mL of this antibody detected phospho-TrkA (Tyr794) in 10 µg of NGF treated human TrkA-transfected PC12 cell lysate.
Usage Statement
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Transactivation of Trk neurotrophin receptors by G-protein-coupled receptor ligands occurs on intracellular membranes. Rajagopal, R; Chen, ZY; Lee, FS; Chao, MV The Journal of neuroscience : the official journal of the Society for Neuroscience
24
6650-8
2004
Neurotrophins, such as NGF and BDNF, activate Trk receptor tyrosine kinases through receptor dimerization at the cell surface followed by autophosphorylation and intracellular signaling. It has been shown that activation of Trk receptor tyrosine kinases can also occur via a G-protein-coupled receptor (GPCR) mechanism, without involvement of neurotrophins. Two GPCR ligands, adenosine and pituitary adenylate cyclase-activating polypeptide (PACAP), can activate Trk receptor activity to increase the survival of neural cells through stimulation of Akt activity. To investigate the mechanism of Trk receptor transactivation, we have examined the localization of Trk receptors in PC12 cells and primary neurons after treatment with adenosine agonists and PACAP. In contrast to neurotrophin treatment, Trk receptors were sensitive to transcriptional and translational inhibitors, and they were found predominantly in intracellular locations particularly associated with Golgi membranes. Biotinylation and immunostaining experiments confirm that most of the transactivated Trk receptors are found in intracellular membranes. These results indicate that there are alternative modes of activating Trk receptor tyrosine kinases in the absence of neurotrophin binding at the cell surface and that receptor signaling may occur and persist inside of neuronal cells.
