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Macrophage Receptor with Collagenous Structure ELISA Kit, Colorimetric (MTS-1123-HM42)

Overview

Description
Creative Biolabs provides sandwich ELISA kit for quantitative measurement of Macrophage Receptor with Collagenous Structure 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 Samples, Plasma, Serum, Tissue Lysate
Specificity
Macrophage Receptor with Collagenous Structure

Specification

Size
96 tests
Bioassay Target Name
Macrophage Receptor with Collagenous Structure
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 receptor with collagenous structure
Synonyms
SR-A6; SCARA2
Background
The protein encoded by this gene is a member of the class A scavenger receptor family and is part of the innate antimicrobial immune system. The protein may bind both Gram-negative and Gram-positive bacteria via an extracellular, C-terminal, scavenger receptor cysteine-rich (SRCR) domain. In addition to short cytoplasmic and transmembrane domains, there is an extracellular spacer domain and a long, extracellular collagenous domain. The protein may form a trimeric molecule by the association of the collagenous domains of three identical polypeptide chains.
Sub Cat Reactivity Sensitivity Detection Range  
MTS-1123-HM330 Mouse User optimized Inquiry
MTS-1123-HM331 Human User optimized Inquiry
FAQs Customer Reviews Related Products

This receptor is large and domain-rich. How does the assay handle different forms or fragments, and what should I consider if my samples may contain cleavage products?

The target is described as having multiple domains, including a collagenous region and an SRCR-related domain. In ELISA, detection depends on which epitopes the antibody pair recognizes. If cleavage fragments are expected, we recommend validating by comparing a positive control (such as recombinant protein or a known-positive sample) with your experimental samples, and using dilution linearity checks to confirm consistent behavior. If you tell us your context (shedding, protease activity), we can suggest stabilization and interpretation best practices.

We work on bacterial binding and innate antimicrobial pathways. Can this kit support those studies, or is it only for basic expression measurement?

The background information links this receptor to innate antimicrobial functions and bacterial interactions. This kit is best used to quantify protein levels across conditions (stimulation, infection models, polarization states), which can support your mechanism by showing whether expression changes track with phenotype. For direct bacterial-binding function, ELISA is typically paired with complementary assays such as binding/uptake measurements. Many customers combine quantification plus functional readouts to connect expression changes to antimicrobial outcomes.

How do I minimize non-specific binding when my samples include extracellular matrix components or collagen-rich tissues?

Collagen-rich matrices can contribute to higher background if sample preparation is harsh or particulate content is high. We recommend thorough clarification (centrifugation and removal of debris), consistent homogenization methods, and a pilot dilution series to reduce matrix interference. Because this is a colorimetric sandwich ELISA kit, careful wash steps and proper blocking are critical for clean baselines. If you share your tissue type and lysis buffer, we can suggest practical adjustments to improve signal specificity without sacrificing recovery.

  • Good support for complex receptor targets and tissue samples in our inflammation assay pipeline
    We used this kit on tissue homogenates where extracellular matrix content can complicate ELISAs. After implementing suggested clarification and dilution steps, background decreased and the signal became much more interpretable. The kit served our goal of comparing receptor expression across infection-like stimuli rather than mapping exact isoforms. Documentation and support were strong, especially on sample prep considerations for collagen-rich materials.
  • Clear readout for expression changes in innate immunity experiments for routine lab and screening use
    Our study focused on innate immune receptor expression changes after bacterial challenge conditions. The kit produced consistent directional changes across biological replicates, and the colorimetric workflow fit our standard plate reader setup. We appreciated that the supplier explained how domain structure can influence detection and advised validation experiments to interpret fragments or shedding. That guidance helped us present the data responsibly in internal reports.
  • Practical ELISA for screening across multiple stimulation conditions for complex matrices and tight schedules
    We screened multiple macrophage activation conditions and needed a manageable, reliable protein quantification tool. This kit worked well for relative comparisons and helped prioritize conditions for deeper mechanistic work. The assay was straightforward, and technical support offered specific suggestions when we saw increased background in certain homogenate batches. Overall, it's a practical option for labs studying receptor expression within broader innate immune projects.

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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