This product format is designed to support both protein- and mRNA-level readouts in one project plan, so you can trend CCL1 secretion alongside gene expression changes after stimulation or inhibitor treatment. In practice, you can run ELISA on supernatants while running qPCR on matched cell pellets, enabling stronger biological interpretation and easier figure building. We also provide technical support for sample handling and normalization strategy suggestions.
The kit is intended for common research matrices such as cell culture supernatant and other biological fluids or lysates where CCL1 is expected to be present. To minimize matrix effects, we recommend using proper dilution series, including spiked recovery checks, and ensuring consistent sample buffers across your standard curve and unknowns. If you share your sample background and expected concentration range, we can suggest practical dilution starting points and controls.
For time-course or multi-plate studies, reproducibility is improved by using consistent pipetting practice, strict incubation timing, and running internal controls across plates (for example, a pooled reference sample). We recommend building an inter-plate normalization plan before you start, especially when comparing different donors or stimulation conditions. If needed, we can help you plan plate maps, replicate strategy, and acceptance criteria so your longitudinal CCL1 trends remain defensible.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.