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Macrophage Stimulating 1 Receptor ELISA Kit, Colorimetric (MTS-1123-HM44)

Overview

Description
Creative Biolabs provides sandwich ELISA kit for quantitative measurement of Macrophage Stimulating 1 Receptor in different sample types by colorimetric.
Applications
ELISA
Qualified With
Quality Certificate
Detection Method
Colorimetric
Method Type
Sandwich ELISA
Analytical Method
Quantitative
Sample Type
Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Lysate
Specificity
Macrophage Stimulating 1 Receptor

Specification

Size
96 tests
Sample Volume
100 μL
Plate
Pre-coated
Bioassay Target Name
Macrophage Stimulating 1 Receptor
Storage
-20 °C
Storage Comment
Reference to the protocol
Expiry Date
6 months
Product Disclaimer
This product is provided for research only, not suitable for human or animal use.

Target Details

Full Name
macrophage stimulating 1 receptor
Synonyms
RON; SEA; PTK8; CD136; NPCA3; CDw136; p185-Ron
Background
This gene encodes a cell surface receptor for macrophage-stimulating protein (MSP) with tyrosine kinase activity. The mature form of this protein is a heterodimer of disulfide-linked alpha and beta subunits, generated by proteolytic cleavage of a single-chain precursor. The beta subunit undergoes tyrosine phosphorylation upon stimulation by MSP. This protein is expressed on the ciliated epithelia of the mucociliary transport apparatus of the lung, and together with MSP, thought to be involved in host defense. Alternative splicing generates multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.
Sub Cat Reactivity Sensitivity Detection Range  
MTS-1123-HM334 Human User optimized Inquiry
MTS-1123-HM335 Mouse User optimized Inquiry
FAQs Customer Reviews Related Products

We study receptor biology in macrophages and worry about detecting membrane vs soluble forms. How should we interpret results from this colorimetric sandwich ELISA?

This kit is a sandwich ELISA designed for quantitative measurement of Macrophage Stimulating 1 Receptor with a colorimetric readout. In ELISA, what you detect depends on antibody epitope recognition and the form present in your sample (lysate vs supernatant). For membrane-associated receptors, lysates often provide clearer detection, while supernatants may reflect shedding. We recommend running both matrices initially and validating interpretation with controls.

What's your recommended approach if we need to compare primary macrophages and cell lines, where baseline expression levels can be very different?

When comparing primary cells and cell lines, the best practice is to standardize sample input (total protein normalization for lysates) and use consistent dilution schemes so readings sit within the reliable region of the standard curve. Because this kit is quantitative, it supports cross-sample comparisons if assay conditions are controlled. Including a reference sample (e.g., pooled lysate) across plates also helps track variability and improves comparability over time.

Can you support method validation for regulated environments or rigorous internal QA, even if it's RUO?

While the kit is supplied for research use, we can still support robust validation planning: accuracy by spike recovery, precision by repeated runs, and matrix evaluation through dilution linearity. We also help define acceptance criteria aligned with your internal QA framework. If you share your matrix, expected concentration range, and required precision thresholds, we can propose a validation checklist and documentation strategy suitable for stringent internal standards.

  • Quantitative receptor readout that fit our macrophage workflow well for routine lab and screening use
    We needed a protein-level assay for MS1R to complement transcript profiling. The kit ran smoothly on our plate reader and gave a clean standard curve. We tested lysates and saw more consistent detection than supernatants, which aligned with our receptor biology expectations. Technical support was helpful in advising normalization strategies for comparing cell lines and primary macrophages. Overall, it provided dependable quantitative data for our study design.
  • Good reproducibility once we standardized protein normalization for complex matrices and tight schedules
    Early runs showed variability across samples, but once we normalized lysate input by total protein and used a consistent dilution plan, the assay became quite reproducible. The colorimetric endpoint was easy to capture and interpret, and the kit helped us track treatment-driven receptor changes across timepoints. We also appreciated the supplier's recommendations on including a pooled reference control to monitor drift between plates.
  • Solid kit for screening receptor modulation by compounds for consistent, publication-ready reporting
    We screened a small compound set looking for receptor modulation effects. This kit was practical for that purpose because it produced stable readouts and supported direct comparisons across treatment conditions. The workflow is familiar to any ELISA-capable lab, and results were consistent with our orthogonal assays. Support was responsive when we asked about matrix effects and recommended pilot dilutions, which improved signal-to-noise.

For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.

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