anti tropomyosin receptor kinase b trkb (Cell Signaling Technology Inc)
Structured Review
Anti Tropomyosin Receptor Kinase B Trkb, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 118 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/anti+trka+antibody/Phospho-TrkA+(Tyr674%2F675)%2FTrkB+(Tyr706%2F707)+Rabbit+mAb/pm42884630-72-47-53
Average 95 stars, based on 118 article reviews
Images
Related Articles
Immunoprecipitation:Article Title: Sustained GRK2-dependent CREB activation is essential for α 2 -adrenergic receptor-induced PC12 neuronal differentiation. Article Snippet: Many aspects of neuronal development, such as neuronal survival and differentiation, are regulated by the transcription factor cAMP-response element-binding protein (CREB).. We have previously reported that 2-adrenergic receptors (ARs), members of the G protein-coupled receptor (GPCR) superfamily, induce neuronal differentiation of rat pheochromocytoma (PC)-12 cells in a subtype-specific manner, i.e. 2A< 2B< 2C.. Herein, we sought to investigate CREB`s involvement in this Jo ur na l P re -p oo f Western Blot:Article Title: Sustained GRK2-dependent CREB activation is essential for α 2 -adrenergic receptor-induced PC12 neuronal differentiation. Article Snippet: Many aspects of neuronal development, such as neuronal survival and differentiation, are regulated by the transcription factor cAMP-response element-binding protein (CREB).. We have previously reported that 2-adrenergic receptors (ARs), members of the G protein-coupled receptor (GPCR) superfamily, induce neuronal differentiation of rat pheochromocytoma (PC)-12 cells in a subtype-specific manner, i.e. 2A< 2B< 2C.. Herein, we sought to investigate CREB`s involvement in this Jo ur na l P re -p oo f other:Article Title: Neuroblast differentiation during development and in neuroblastoma requires KIF1Bβ-mediated transport of TRKA Article Snippet: Biotinylated proteins were resolved by SDS-PAGE, transferred to a nitrocellulose filter, and immunoblotted with an Membrane:Article Title: NGF-conjugated iron oxide nanoparticles promote differentiation and outgrowth of PC12 cells. Article Snippet: The search for regenerative agents that promote neuronal differentiation and repair is of great importance.. Nerve growth factor (NGF) which is an essential contributor to neuronal differentiation has shown high pharmacological potential for the treatment of central neurodegenerative diseases such as Alzheimer’s and Parkinson’s.. However, growth factors undergo rapid degradation, leading to a short biological half-life. Article Title: Precautionary effects of Red Liriope platyphylla on NGF secretion and Aβ42 deposition under the preclinical stage of Alzheimer's disease in Tg2576 mice Article Snippet: The reaction was then quenched by the addition of 100 μL of stop solution, after which the plates were analyzed by a SoftMax Pro5 spectrophotometer (Molecular Devices, Sunnyvale, CA, USA). .. Proteins prepared from the brain tissues of Non-Tg, vehicle- and AEtRLP-treated Tg2576 mice were separated by electrophoresis on a 10-20% SDS-PAGE gel for 2 h, then transferred to nitrocellulose membranes for 2 h at 40 V. Next, each membrane was incubated separately with one of the following primary antibodies: Article Title: Asparagus cochinchinensis stimulates release of nerve growth factor and abrogates oxidative stress in the Tg2576 model for Alzheimer's disease. Article Snippet: Western blot and slot blot Total protein was prepared from the cortex and hippocampus tissue of mice in subset groups using Pro-Prep Protein Extraction Solution (iNtRON Biotechnology, Seongnam, Korea), then quantified using a SMARTTM BCA Protein Assay Kit (Thermo Scientific, Waltham, MA, USA) for Western blot analysis. .. Briefly, these proteins were separated by 4–20% sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDS-PAGE) for 2 h, after which resolved proteins were transferred to nitrocellulose membranes for 2 h at 40 V. Each membrane was then incubated separately at 4 °C with the following primary antibodies overnight: Article Title: Asparagus cochinchinensis stimulates release of nerve growth factor and abrogates oxidative stress in the Tg2576 model for Alzheimer’s disease Article Snippet: Total protein was prepared from the cortex and hippocampus tissue of mice in subset groups using Pro-Prep Protein Extraction Solution (iNtRON Biotechnology, Seongnam, Korea), then quantified using a SMARTTM BCA Protein Assay Kit (Thermo Scientific, Waltham, MA, USA) for Western blot analysis. .. Briefly, these proteins were separated by 4–20% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) for 2 h, after which resolved proteins were transferred to nitrocellulose membranes for 2 h at 40 V. Each membrane was then incubated separately at 4 °C with the following primary antibodies overnight: Incubation:Article Title: Evaluation of NTRK Fusions Detection Method in Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma Article Snippet: .. After rinsing in PBS, the sections were incubated with ananti-pan-TRK antibody (# EPR17341 ; 1:50 dilution; Abcam, Cambridge, UK), Article Title: Precautionary effects of Red Liriope platyphylla on NGF secretion and Aβ42 deposition under the preclinical stage of Alzheimer's disease in Tg2576 mice Article Snippet: The reaction was then quenched by the addition of 100 μL of stop solution, after which the plates were analyzed by a SoftMax Pro5 spectrophotometer (Molecular Devices, Sunnyvale, CA, USA). .. Proteins prepared from the brain tissues of Non-Tg, vehicle- and AEtRLP-treated Tg2576 mice were separated by electrophoresis on a 10-20% SDS-PAGE gel for 2 h, then transferred to nitrocellulose membranes for 2 h at 40 V. Next, each membrane was incubated separately with one of the following primary antibodies: Article Title: Asparagus cochinchinensis stimulates release of nerve growth factor and abrogates oxidative stress in the Tg2576 model for Alzheimer's disease. Article Snippet: Western blot and slot blot Total protein was prepared from the cortex and hippocampus tissue of mice in subset groups using Pro-Prep Protein Extraction Solution (iNtRON Biotechnology, Seongnam, Korea), then quantified using a SMARTTM BCA Protein Assay Kit (Thermo Scientific, Waltham, MA, USA) for Western blot analysis. .. Briefly, these proteins were separated by 4–20% sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDS-PAGE) for 2 h, after which resolved proteins were transferred to nitrocellulose membranes for 2 h at 40 V. Each membrane was then incubated separately at 4 °C with the following primary antibodies overnight: Article Title: Asparagus cochinchinensis stimulates release of nerve growth factor and abrogates oxidative stress in the Tg2576 model for Alzheimer’s disease Article Snippet: Total protein was prepared from the cortex and hippocampus tissue of mice in subset groups using Pro-Prep Protein Extraction Solution (iNtRON Biotechnology, Seongnam, Korea), then quantified using a SMARTTM BCA Protein Assay Kit (Thermo Scientific, Waltham, MA, USA) for Western blot analysis. .. Briefly, these proteins were separated by 4–20% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) for 2 h, after which resolved proteins were transferred to nitrocellulose membranes for 2 h at 40 V. Each membrane was then incubated separately at 4 °C with the following primary antibodies overnight: Electrophoresis:Article Title: Precautionary effects of Red Liriope platyphylla on NGF secretion and Aβ42 deposition under the preclinical stage of Alzheimer's disease in Tg2576 mice Article Snippet: The reaction was then quenched by the addition of 100 μL of stop solution, after which the plates were analyzed by a SoftMax Pro5 spectrophotometer (Molecular Devices, Sunnyvale, CA, USA). .. Proteins prepared from the brain tissues of Non-Tg, vehicle- and AEtRLP-treated Tg2576 mice were separated by electrophoresis on a 10-20% SDS-PAGE gel for 2 h, then transferred to nitrocellulose membranes for 2 h at 40 V. Next, each membrane was incubated separately with one of the following primary antibodies: SDS Page:Article Title: Precautionary effects of Red Liriope platyphylla on NGF secretion and Aβ42 deposition under the preclinical stage of Alzheimer's disease in Tg2576 mice Article Snippet: The reaction was then quenched by the addition of 100 μL of stop solution, after which the plates were analyzed by a SoftMax Pro5 spectrophotometer (Molecular Devices, Sunnyvale, CA, USA). .. Proteins prepared from the brain tissues of Non-Tg, vehicle- and AEtRLP-treated Tg2576 mice were separated by electrophoresis on a 10-20% SDS-PAGE gel for 2 h, then transferred to nitrocellulose membranes for 2 h at 40 V. Next, each membrane was incubated separately with one of the following primary antibodies: Nucleic Acid Electrophoresis:Article Title: Asparagus cochinchinensis stimulates release of nerve growth factor and abrogates oxidative stress in the Tg2576 model for Alzheimer's disease. Article Snippet: Western blot and slot blot Total protein was prepared from the cortex and hippocampus tissue of mice in subset groups using Pro-Prep Protein Extraction Solution (iNtRON Biotechnology, Seongnam, Korea), then quantified using a SMARTTM BCA Protein Assay Kit (Thermo Scientific, Waltham, MA, USA) for Western blot analysis. .. Briefly, these proteins were separated by 4–20% sodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDS-PAGE) for 2 h, after which resolved proteins were transferred to nitrocellulose membranes for 2 h at 40 V. Each membrane was then incubated separately at 4 °C with the following primary antibodies overnight: Article Title: Asparagus cochinchinensis stimulates release of nerve growth factor and abrogates oxidative stress in the Tg2576 model for Alzheimer’s disease Article Snippet: Total protein was prepared from the cortex and hippocampus tissue of mice in subset groups using Pro-Prep Protein Extraction Solution (iNtRON Biotechnology, Seongnam, Korea), then quantified using a SMARTTM BCA Protein Assay Kit (Thermo Scientific, Waltham, MA, USA) for Western blot analysis. .. Briefly, these proteins were separated by 4–20% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) for 2 h, after which resolved proteins were transferred to nitrocellulose membranes for 2 h at 40 V. Each membrane was then incubated separately at 4 °C with the following primary antibodies overnight: |

