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Macrophage Chemokine Ligand 16 (CCL16) Competition ELISA Kit (MTS-1123-HM97)

Overview

Description
Creative Biolabs provides competition ELISA kit for quantitative measurement of Chemokine Ligand 16 (CCL16) in different sample types by colorimetric.
Applications
ELISA
Qualified With
Quality Certificate
Reactivity
Human
Detection Method
Colorimetric
Method Type
Competition ELISA
Analytical Method
Quantitative
Sensitivity
1.0 pg/mL
Sample Type
Cell Culture Supernatant, Plasma, Serum, Tissue Homogenate
Specificity
Chemokine Ligand 16 (CCL16)

Specification

Size
96 tests
Detection Range
100-2500 pg/mL
Sample Volume
100 μL
Assay Time
1.5 h
Plate
Pre-coated
Bioassay Target Name
Chemokine Ligand 16 (CCL16)
Storage
4 °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
C-C motif chemokine ligand 16
Synonyms
LEC; LMC; NCC4; CKb12; HCC-4; LCC-1; Mtn-1; NCC-4; SCYL4; ILINCK; SCYA16
Background
This gene is one of several cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for lymphocytes and monocytes but not for neutrophils. This cytokine also shows a potent myelosuppressive activity and suppresses proliferation of myeloid progenitor cells. The expression of this gene is upregulated by IL-10.
FAQs Customer Reviews Related Products

Why would I choose a competition ELISA for CCL16 instead of a standard sandwich ELISA format?

Competition ELISA can be beneficial when the assay design needs a competitive binding approach to quantify the target, sometimes offering flexibility in certain detection constraints. The key is choosing the format that best matches your sample matrix and expected concentration range. If you are measuring CCL16 in samples with challenging backgrounds or if you need a format aligned to your existing validation strategy, competition ELISA may be appropriate. We can help compare formats based on your sample type and goals.

Can I use this kit for multiple sample types in the same study, such as serum and tissue homogenate, and still compare results?

You can, but we strongly recommend validating each matrix using dilution linearity and spike-and-recovery checks because different matrices can shift apparent concentration. Once each matrix is validated and you use consistent dilution rules, you can compare within a matrix reliably and interpret across matrices more cautiously. Including matrix-matched standards or consistent reference samples also improves confidence. If you describe your sample types, we can recommend an efficient validation approach.

What practical steps ensure reliable quantification in a competition ELISA workflow?

Competition ELISA is sensitive to consistent timing and mixing, so we recommend preparing reagents carefully, using calibrated pipettes, and keeping incubation timing identical across wells. Run duplicates, place standards strategically, and include one repeated control sample across plates if you're doing multiple runs. Also ensure thorough washing to reduce non-specific signal. Our technical support can help you set acceptance criteria for curve shape and replicate agreement before you scale up.

  • Competition format worked well after careful control setup and timing
    We selected the competition ELISA to align with our internal assay strategy and found it produced consistent results once we standardized incubation timing and washing. The key for us was adding a repeated control sample across plates and running duplicates for critical samples. After that, variability decreased and trends matched what we expected biologically. It required a bit more discipline in execution, but it paid off in data quality.
  • Useful for quantification in a mixed-sample project with validation steps
    We measured CCL16 across two matrices in one project and used dilution linearity and spike recovery to confirm performance. Once validated, the assay produced stable readouts and helped us compare treatment responses within each sample type. The protocol was clear enough for experienced staff, and vendor support was helpful when we asked about interpreting curve behavior. Overall, it's a solid choice if you're willing to validate your matrices properly.
  • Good assay once optimized, and support helped us avoid common pitfalls
    Our first run had higher variability than expected, but support suggested changes to timing consistency and wash technique, which improved replicates significantly. After we implemented their recommendations and used a pooled reference, the assay became reliable for our study. The competition format is slightly less forgiving than simpler assays, but it can deliver strong results when executed carefully. We would use it again for controlled experimental runs.

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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