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- Table of Contents
Facts about Fibroblast growth factor receptor substrate 2.
Modulates indicating via SHC1 by competing for a common binding site on NTRK1. .
Human | |
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Gene Name: | FRS2 |
Uniprot: | Q8WU20 |
Entrez: | 10818 |
Belongs to: |
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No superfamily |
FGFR signalling adaptor; FGFR-signaling adaptor SNT; fibroblast growth factor receptor substrate 2; FRS2; FRS2A; FRS2alpha; SNT; SNT1; SNT-1FGFR substrate 2; Suc1-associated neurotrophic factor target 1
Mass (kDA):
57.029 kDA
Human | |
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Location: | 12q15 |
Sequence: | 12; NC_000012.12 (69470371..69579793) |
Highly expressed in heart, brain, spleen, lung, liver, skeletal muscle, kidney and testis.
Endomembrane system. Cytoplasmic, membrane-bound.
This article will focus on the Boster Bio Anti-FRS2 Marker & High-affinity Primary Antibody. It will also address the Cell-based ELISA system. It will help you decide which one is best suited for your research needs. Compare the benefits and disadvantages of each kit against their respective purposes. You will need to decide which one is best for your specific application.
FRS2 is a phosphoprotein that is expressed in cells, and microbial species. There are two types that react with this protein. One type reacts with mouse cells and the other is specific to human cells. The flow procedures will vary depending on which FRS2 antibody is being used. Boster Bio provides high-affinity primary antibodies that have been validated by Western Blotting, Immunohistochemistry, and ELISA.
When designing an antigen specific antibody, the first thing a biologist should look at is its affinity. High affinity is desirable but not always necessary. This property could make it more difficult to separate the antigen from the antibody, and therefore requires more aggressive methods for elution. Researchers will be able to develop a high-affinity primary antibodies by using the FRS2 marker.
Researchers need to understand the interaction between these molecules in order develop high-affinity prima antibodies. Molecular imaging can use antibody fragments as professional tools to study protein–protein and RNA–protein interactions. For example, researchers are creating new imaging methods to assess the efficacy of therapy. mAbs are known for having a high serum half life and low tumor penetration. Thus, smaller antibody fragments are needed to circumvent these limitations. This is called Nb labeling.
To determine the affinity a monoclonal immunoglobulin to a particular ligand it must be measured using the ratio between dissociation and affinity constant (KD), values of antibodies and proteins. The KD value is generally lower, which indicates that the monoclonal anti antibody has a greater affinity for a particular ligand. Scientists from Abcam analysed the OI-RD data at UC Davis.
The FRS2 marker makes it easy to develop high-affinity primaries antibodies with an optimized antigen binding domain. Single-domain antibodies exhibit low affinity, poor solubility and high production costs but they retain the high affinity properties of the parent Ab. Monoclonal Abs with high-affinity monoclonal antibody performance can be enhanced by using monoclonal Abs with high-affinity monoclonal antibodies.
ELISA test confirmed that the MBP-Lk–scFv antibody was able to bind to the IFN–g-antigen. Western blot analysis confirmed MBP-Lk–scFv binding to the IFN–g standard antigen. This indicates that the monoclonal immunoglobulin is highly active in binding antigens. This affinity constant is 2.6x109 L/mol.
Boster Bio FRS2 cell based antibody ELISA kit allows for fast and accurate analysis of the phosphorylation status Fra-2 proteins in cultured cells. This kit can be used for monitoring the relative levels in cell culture of Fra-2 proteins and to screen for activators and inhibitors of the target proteins. It is therefore suitable for screening a wide range of treatments.
PMID: 9660748 by Xu H., et al. Novel recognition motif on fibroblast growth factor receptor mediates direct association and activation of SNT adapter proteins.
PMID: 10092678 by Meakin S.O., et al. The signaling adapter FRS-2 competes with Shc for binding to the nerve growth factor receptor TrkA. A model for discriminating proliferation and differentiation.