Key Product Details

Species Reactivity

Validated:

Human

Cited:

Human

Applications

Validated:

Immunohistochemistry, Western Blot, Blockade of Receptor-ligand Interaction, Flow Cytometry, Simple Western, CyTOF-ready

Cited:

Immunohistochemistry, Immunocytochemistry, Functional Assay

Label

Unconjugated

Antibody Source

Polyclonal Goat IgG
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Product Specifications

Immunogen

Mouse myeloma cell line NS0-derived recombinant human TrkC
Cys32-Asp428
Accession # Q96CY4

Specificity

Detects human TrkC in direct ELISAs and Western blots. In direct ELISAs and Western blots, less than 1% cross-reactivity with recombinant human TrkB is observed.

Clonality

Polyclonal

Host

Goat

Isotype

IgG

Endotoxin Level

<0.10 EU per 1 μg of the antibody by the LAL method.

Scientific Data Images for Human TrkC Antibody

Detection of HAF017 TrkC antibody by Western Blot.

Detection of HAF017 TrkC by Western Blot.

Western blot shows lysates of human brain (cerebellum) tissue, human brain (hippocampus) tissue, human brain (hypothalamus) tissue, and human brain stem tissue. PVDF membrane was probed with 1 µg/mL of Goat Anti-Human TrkC Antigen Affinity-purified Polyclonal Antibody (Catalog # AF373) followed by HRP-conjugated Anti-Goat IgG Secondary Antibody (HAF017). Specific bands were detected for TrkC at approximately 140, 95 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.

Detection of Human TrkC antibody by Simple WesternTM.

Detection of Human TrkC by Simple WesternTM.

Simple Western lane view shows lysates of human brain (hypothalamus) tissue, loaded at 0.2 mg/mL. A specific band was detected for TrkC at approximately 164 kDa (as indicated) using 10 µg/mL of Goat Anti-Human TrkC Antigen Affinity-purified Polyclonal Antibody (Catalog # AF373) followed by 1:50 dilution of HRP-conjugated Anti-Goat IgG Secondary Antibody (HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.

Detection of TrkC in A549 cells by Flow Cytometry

A549 cells were stained with Goat Anti-Human TrkC Antigen Affinity-purified Polyclonal Antibody (Catalog # AF373, filled histogram) or isotype control antibody (Catalog # 4-001-A, open histogram) followed by Phycoerythrin-conjugated Anti-Goat IgG Secondary Antibody (Catalog # F0107). View our protocol for Staining Membrane-associated Proteins.

Detection of TrkC by Immunohistochemistry

Detection of TrkC by Immunohistochemistry

Characterization of immunopanned SNs. (A) Representative immunofluorescence images of immunopanned SNs. Cells were fixed 20 days post panning (day 45) and stained for the indicated antibodies. DAPI was used to mark the nucleus. Arrows indicate neurons. (B–D) Quantification of IF images from panned SNs using anti-TRKA antibody (B), anti-TRKB (C), and anti-TRKC (D) antibodies. Non-neurons are cells that are positive for DAPI but do not express any of the TRK receptors. (E) Representative images of TRKC-panned SNs expressing TRKB and TRKC. Arrows indicate TRKB+TRKC+ neurons. n = 4–8 biological replicates. Graphs show mean ± S.D. One-way ANOVA was used. ns, non-significant, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37206924), licensed under a CC-BY license. Not internally tested by R&D Systems.
Detection of TrkC by Immunohistochemistry

Detection of TrkC by Immunohistochemistry

Characterization of immunopanned SNs. (A) Representative immunofluorescence images of immunopanned SNs. Cells were fixed 20 days post panning (day 45) and stained for the indicated antibodies. DAPI was used to mark the nucleus. Arrows indicate neurons. (B–D) Quantification of IF images from panned SNs using anti-TRKA antibody (B), anti-TRKB (C), and anti-TRKC (D) antibodies. Non-neurons are cells that are positive for DAPI but do not express any of the TRK receptors. (E) Representative images of TRKC-panned SNs expressing TRKB and TRKC. Arrows indicate TRKB+TRKC+ neurons. n = 4–8 biological replicates. Graphs show mean ± S.D. One-way ANOVA was used. ns, non-significant, ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37206924), licensed under a CC-BY license. Not internally tested by R&D Systems.

Applications for Human TrkC Antibody

Application
Recommended Usage

Blockade of Receptor-ligand Interaction

In a functional ELISA, 1-3 µg/mL of this antibody will block 50% of the binding of 5 ng/mL of Recombinant Human NT-3 (Catalog # 267-N3) to immobilized Recombinant Human TrkC Fc Chimera (Catalog # 373-TC) coated at 1 µg/mL (100 µL/well). At 30 μg/mL, this antibody will block >90% of the binding.

CyTOF-ready

Ready to be labeled using established conjugation methods. No BSA or other carrier proteins that could interfere with conjugation.

Flow Cytometry

0.25 µg/106 cells
Sample: Human TrkC transfected Baf/3 cells; A549 human lung carinoma cell line

Immunohistochemistry

5-15 µg/mL
Sample: Immersion fixed paraffin-embedded sections of human brain (hippocampus) and perfusion fixed frozen sections of mouse brain (cortex)

Simple Western

10 µg/mL
Sample: Human brain (hypothalamus) tissue

Western Blot

1 µg/mL
Sample: Human brain (cerebellum) tissue, human brain (hippocampus) tissue, human brain (hypothalamus) tissue, and human brain stem tissue.

Flow Cytometry Panel Builder

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Save time and reduce costly mistakes by quickly finding compatible reagents using the Panel Builder Tool.

Advanced Features

  • Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
  • Spillover Popups - Visualize the spectra of individual fluorochromes
  • Antigen Density Selector - Match fluorochrome brightness with antigen density
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Formulation, Preparation, and Storage

Purification

Antigen Affinity-purified

Reconstitution

Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.


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Formulation

Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.

Shipping

Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.

Stability & Storage

Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

Calculators

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

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Background: TrkC

The neurotrophins, including NGF, BDNF, NT-3 and NT-4/5, constitute a group of structurally related, secreted proteins that play an important role in the development and function of the nervous system. The biological activities of the neurotrophins are mediated by binding to and activating two unrelated receptor types: the p75 neurotrophin receptor (p75NTR) and the Trk family of receptor tyrosine kinases (1, 2). P75NTR is a member of the tumor necrosis factor receptor superfamily (TNFRSF) and has been designated TNFRSF16. It binds all neurotrophins with low-affinity to transduce cellular signaling pathways that synergize or antagonize those activated by the Trk receptors. Three Trk family proteins, TrkA, TrkB and TrkC, exhibiting different ligand specificities, have been identified. TrkA binds NGF and NT‑3, TrkB binds BDNF, NT-3 and NT-4/5, and TrkC only binds NT-3 (1, 2). All Trk family proteins share a conserved, complex subdomain organization consisting of a signal peptide, two cysteine-rich domains, a cluster of three leucine-rich motifs, and two immunoglobulin-like domains in the extracellular region, as well as an intracellular region that contains the tyrosine kinase domain (3). Natural splice variants of the different Trks, lacking the first cysteine-rich domain, the first and second or all three of the leucine-rich motifs, or the tyrosine kinase domain, have been described (4). At the protein sequence level, Trks are highly conserved between species with the extracellular domains of human and mouse TrkC's showing 94% amino acid sequence identity (5). The proteins also exhibit cross-species activity. The primary location of TrkC expression is in the nervous system and, specifically, in regions of the CNS. Low level TrkC expression has also been observed in a wide variety of tissues outside the nervous system (6).

References

  1. Huang, E.J. and L.F. Reichardt. (2003) Annu. Rev. Biochem. 72:(epub ahead of print).
  2. Dechant, G. (2001) Cell Tissue Res. 305:229.
  3. Schneider, R. and M. Schweiger (1991) Oncogene 6:1807.
  4. Ninkina, N. et al. (1997) J. Biol. Chem. 272:13019.
  5. Menn, B. et al. (1998) J. Comp. Neurol. 401:47.
  6. Shelton, D. et al. (1995) J. Neurosci. 15:477.

Long Name

Neurotrophic Tyrosine Kinase Receptor C

Alternate Names

NTRK3

Entrez Gene IDs

4916 (Human); 18213 (Mouse); 29613 (Rat)

Gene Symbol

NTRK3

UniProt

Additional TrkC Products

Product Documents for Human TrkC Antibody

Certificate of Analysis

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Note: Certificate of Analysis not available for kit components.

Product Specific Notices for Human TrkC Antibody

For research use only

Related Research Areas

Citations for Human TrkC Antibody

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Protocols

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