TrkB [p Tyr816] Antibody - Azide and BSA Free
Novus Biologicals | Catalog # NBP1-03499
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Key Product Details
Species Reactivity
Validated:
Human, Mouse, Rat
Cited:
Human, Mouse, Rat
Applications
Validated:
Immunohistochemistry, Immunohistochemistry-Paraffin, Immunohistochemistry-Frozen, Western Blot, Immunocytochemistry/ Immunofluorescence
Cited:
Immunohistochemistry-Frozen, Western Blot, Immunocytochemistry/ Immunofluorescence, IF/IHC
Label
Unconjugated
Antibody Source
Polyclonal Rabbit IgG
Format
Azide and BSA Free
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Product Specifications
Immunogen
A synthetic peptide from the region around (and including) phospho-Tyr816 site of rat TrkB conjugated to an immunogenic carrier protein was used as the immunogen. The peptide is homologous in human and mouse.
Modification
p Tyr816
Localization
subcellular location: membrane; single-pass type i membrane protein.
Clonality
Polyclonal
Host
Rabbit
Isotype
IgG
Description
Novus Biologicals Rabbit TrkB [p Tyr816] Antibody - Azide and BSA Free (NBP1-03499) is a polyclonal antibody validated for use in IHC, WB and ICC/IF. Anti-TrkB Antibody: Cited in 14 publications. All Novus Biologicals antibodies are covered by our 100% guarantee.
Scientific Data Images for TrkB [p Tyr816] Antibody - Azide and BSA Free
Immunocytochemistry/ Immunofluorescence: TrkB [p Tyr816] Antibody [NBP1-03499]
TrkB-[p-Tyr816]-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-03499-img0001.jpgWestern Blot: TrkB [p Tyr816] Antibody - Azide and BSA Free [NBP1-03499] -
BDNF and TrkB in the L4-L6 SCDH plays a key role in the hyperalgesic priming model. (A-B) The quantification of the Western blots results and a representative Western blot showing BDNF and p-TrkB protein isolated from the ipsilateral SCDH 48 h after 2nd injection. (C) Representative immunofluorescence images of BDNF (red) merged with p-TrkB (green) in ipsilateral L4-6 SCDH of hyperalgesic priming rats. (D-F) The immunofluorescence quantification of BDNF and p-TrkB co-expression cells in ipsilateral L4-6 SCDH. (G-H) Evaluation of BDNF and p-TrkB gene expression in ipsilateral L4-6 SCDH using qPCR in the sHP, HP, HP + EA, HP + sEA groups 48 h after 2nd injection. Data are presented as mean +/- SEM, n = 5; *p < 0.05, **p < 0.01 vs sHP group, #p < 0.05, ##p < 0.01 vs HP group. Two-way ANOVA with Tukey's post-hoc test was applied in. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.) Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36875547), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: TrkB [p Tyr816] Antibody - Azide and BSA Free [NBP1-03499] -
BDNF neutralizing antibody intervention reduced phosphorylation of TrkB. (A-B) The quantification of the Western blots results and a representative Western blot showing BDNF and p-TrkB protein isolated from the ipsilateral SCDH 48 h after 2nd injection. (C) Representative immunofluorescence images of BDNF (red) merged with p-TrkB (green) in ipsilateral L4-6 SCDH of BDNF neutralizing antibody intervention rats. (D-F) The immunofluorescence quantification of BDNF and p-TrkB co-expression cells in ipsilateral L4-6 SCDH. (G-H) Evaluation of BDNF and p-TrkB gene expression in ipsilateral L4-6 SCDH using qPCR in the sHP + IgG, HP + IgG, HP + BDNF neutralizing antibody groups 48 h after 2nd injection. Data are presented as mean +/- SEM, n = 5; *p < 0.05, **p < 0.01 vs sHP + IgG group, #p < 0.05, ##p < 0.01 vs HP + IgG group. Two-way ANOVA with Tukey's post-hoc test was applied in. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.) Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36875547), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: TrkB [p Tyr816] Antibody - Azide and BSA Free [NBP1-03499] -
BDNF recombinant protein intervention increased phosphorylation of TrkB. (A-B) The quantification of the Western blots results and a representative Western blot showing BDNF and p-TrkB protein isolated from the ipsilateral SCDH 48 h after 2nd injection. (C) Representative immunofluorescence images of BDNF (red) merged with p-TrkB (green) in ipsilateral L4-6 SCDH of BDNF recombinant protein intervention rats. (D-F) The immunofluorescence quantification of BDNF and p-TrkB co-expression cells in ipsilateral L4-6 SCDH. (G-H) Evaluation of BDNF and p-TrkB gene expression in ipsilateral L4-6 SCDH using qPCR in the HP + PBS, HP + EA + PBS, HP + EA + BDNF groups 48 h after 2nd injection. Data are presented as mean +/- SEM, n = 5; *p < 0.05, **p < 0.01 vs HP + PBS group, #p < 0.05, ##p < 0.01 vs HP + EA + PBS group. Two-way ANOVA with Tukey's post-hoc test was applied in. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.) Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36875547), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: TrkB [p Tyr816] Antibody - Azide and BSA Free [NBP1-03499] -
The expression of BDNF-TrkB signaling in the SDH of CYP-induced cystitis. a Changes of the mechanical threshold in CYP-induced cystitis model. Compared to that in the control group, the mechanical threshold of the cystitis group decreased significantly after the CYP injection and remained low until day 17, and the minimum threshold value was reached on day 12. The expression of b BDNF, c TrkB, and dp-TrkB were evaluated by western blots. Compared to the control group, they were upregulated on days 8, 12, and 17. e Immunofluorescence double staining assay of BDNF and p-TrkB in the SDH. BDNF and p-TrkB (red), NeuN, GFAP, and OX-42( green), co-localization (yellow). BDNF was mainly colocalized in neurons which mainly located in Laminate II to IV. And TrkB receptors expressed in neurons, microglia, and astrocytes. The white dotted lines in picture “BDNF/NeuN" showed the laminate of the SDH according to Rexed and Steiner. Scale bar = 100 μm. All data were calculated as mean +/- SEM (n = 5 per group). *p < 0.05, ** p < 0.01, *** p < 0.001 vs. the control group Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/31931832), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: TrkB [p Tyr816] Antibody - Azide and BSA Free [NBP1-03499] -
The effect of GSB-106 on the BDNF content and the site-specific phosphorylation of TrkB receptor in the prefrontal cortex and the hippocampus of mice subjected to UCMS. (a) BDNF, (b) pTrkB(Tyr706/707), (c) pTrkB(Tyr816), (d) pTrkB(Tyr515) proteins expression in mice prefrontal cortex and hippocampus. After the completion of UCMS procedure and the compound treatment, mice were decapitated and brain structures were collected. Protein extracts were subjected to polyacrylamide gel electrophoresis and transferred for Western blotting. Blots were probed with anti-BDNF, anti-phosphorylated TrkB antibodies and then reprobed with anti-TrkB antibody, anti-a-tubulin antibodies. For every picture, representative images for immunoblots are shown on the top panels, and quantitative data are shown on the bottom panels (red dots on the graphs correspond to mice 4, 8, 10 and 15; dark dots are all mice samples in the group). All data are expressed as mean +/- SEM (n = 3; the significance of intergroup differences was estimated by one-way analysis of the variance (ANOVA), followed by Tukey’s multiple comparisons test). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/34948177), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: TrkB [p Tyr816] Antibody - Azide and BSA Free [NBP1-03499] -
BDNF and TrkB in the L4-L6 SCDH plays a key role in the hyperalgesic priming model. (A-B) The quantification of the Western blots results and a representative Western blot showing BDNF and p-TrkB protein isolated from the ipsilateral SCDH 48 h after 2nd injection. (C) Representative immunofluorescence images of BDNF (red) merged with p-TrkB (green) in ipsilateral L4-6 SCDH of hyperalgesic priming rats. (D-F) The immunofluorescence quantification of BDNF and p-TrkB co-expression cells in ipsilateral L4-6 SCDH. (G-H) Evaluation of BDNF and p-TrkB gene expression in ipsilateral L4-6 SCDH using qPCR in the sHP, HP, HP + EA, HP + sEA groups 48 h after 2nd injection. Data are presented as mean +/- SEM, n = 5; *p < 0.05, **p < 0.01 vs sHP group, #p < 0.05, ##p < 0.01 vs HP group. Two-way ANOVA with Tukey's post-hoc test was applied in. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.) Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36875547), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: TrkB [p Tyr816] Antibody - Azide and BSA Free [NBP1-03499] -
BDNF recombinant protein intervention increased phosphorylation of TrkB. (A-B) The quantification of the Western blots results and a representative Western blot showing BDNF and p-TrkB protein isolated from the ipsilateral SCDH 48 h after 2nd injection. (C) Representative immunofluorescence images of BDNF (red) merged with p-TrkB (green) in ipsilateral L4-6 SCDH of BDNF recombinant protein intervention rats. (D-F) The immunofluorescence quantification of BDNF and p-TrkB co-expression cells in ipsilateral L4-6 SCDH. (G-H) Evaluation of BDNF and p-TrkB gene expression in ipsilateral L4-6 SCDH using qPCR in the HP + PBS, HP + EA + PBS, HP + EA + BDNF groups 48 h after 2nd injection. Data are presented as mean +/- SEM, n = 5; *p < 0.05, **p < 0.01 vs HP + PBS group, #p < 0.05, ##p < 0.01 vs HP + EA + PBS group. Two-way ANOVA with Tukey's post-hoc test was applied in. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.) Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36875547), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for TrkB [p Tyr816] Antibody - Azide and BSA Free
Application
Recommended Usage
Immunocytochemistry/ Immunofluorescence
1:10-1:500
Immunohistochemistry
10-50 ug/ml
Immunohistochemistry-Frozen
10-50 ug/ml
Immunohistochemistry-Paraffin
10-50 ug/ml
Western Blot
10-50 ug/ml
Application Notes
This antibody has been used in IHC-Frozen as reported in scientific literature (PMID: 23432085), ICC/IF reported in scientific literature (PMID: 23658180).
Formulation, Preparation, and Storage
Purification
Ammonium sulfate precipitation
Reconstitution
Reconstitute 0.5 mg size in 0.5 ml of sterile water. Centrifuge to remove any insoluble material. Glycerol may be added (1:1) for additional stability. Please note the 0.1 mg size is provided in reconstituted format.
Formulation
Lyophilized from PBS
Format
Azide and BSA Free
Preservative
No Preservative
Concentration
Please see the vial label for concentration. If unlisted please contact technical services.
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Calculators
Background: TrkB
Long Name
Neurotrophic Tyrosine Kinase Receptor B
Alternate Names
NTRK2
Gene Symbol
NTRK2
UniProt
Additional TrkB Products
Product Documents for TrkB [p Tyr816] Antibody - Azide and BSA Free
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for TrkB [p Tyr816] Antibody - Azide and BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for TrkB [p Tyr816] Antibody - Azide and BSA Free
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
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