CCL17 Western Blot Experimental Design Guide

Expected bands, documented protocol parameters, controls and antibodies — the at-a-glance facts below, then the full design guide.

Must know before running
Expected band 10.5 kDa
Observed band Not reported — verify product WB image
Gel 15%
Positive control ⓘ Cerebellum
Negative control ⓘ Soft tissue
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass10.5 kDa
ⓘLocalizationSecreted
ⓘProcessing / PTMRecord-dependent
ⓘReactivityMouse

Sample controls for CCL17 Western blot

🧪Use Cerebellum as the first positive-control candidate and Soft tissue as the HPA Not detected negative candidate.
Positive control: Cerebellum (Medium)
Negative control: Soft tissue (Not detected)
HPA protein score determines control status; other expression data is supporting context only.

HPA tissue expression evidence for CCL17

Comprehensive Human Protein Atlas IHC scoring per tissue. Rows are taken directly from the HPA tissue chart on each tissue page — click any row's HPA link to view the source.

Positive expression · recommended positive controls

Tissue Cell type Level Evidence Source
Cerebellum Reported tissue cells Medium Protein (HPA) HPA →
Breast Reported tissue cells Medium Protein (HPA) HPA →
Appendix Reported tissue cells Medium Protein (HPA) HPA →
Bone marrow Reported tissue cells Medium Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Soft tissue Reported tissue cells Not detected Protein (HPA) HPA →
Adipose tissue Reported tissue cells Not detected Protein (HPA) HPA →
Section 1

What Is the Expected CCL17 Western Blot Band Size?

Use the product-observed 10.5 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
10.5 kDaMatches the authoritative product WB observation.
10.5 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected CCL17 appearancePlan around 10.5 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band10.5 kDa; use this as the primary experimental expectation.
Calculated mass10.5 kDa from UniProt Q92583; retain as context.
Gel selection15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PB9031.
Why is my band missing or off?
SituationLikely causeNext action
10.5 kDaMatches the authoritative product WB observation.Confirm with orthogonal controls and the linked product record.
Additional bandMay reflect processing, modification, or non-specific signal.Run a dilution series and compare positive/negative controls.
Weak signalTarget abundance or transfer may be limiting.Verify transfer, increase positive-control abundance, and bracket exposure.
Section 2

Real Curated CCL17 Western Blot Protocols

Start with the molecular-weight rule, then compare verified publication-derived conditions.

Recommended Western blot protocol parameters
Sample / lysateAppendix
Gel %15%
Load20-30 µg total protein per lane
TransferSemi-dry, short transfer
Membrane0.2 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryPB9031 at datasheet starting dilution
Primary incubationOvernight at 4 °C with gentle agitation
SecondarySpecies-matched HRP conjugate at validated dilution
Wash3 × 5 min in TBST
DetectionChemiluminescent substrate
ExposureBracket exposures to avoid saturation
Section 4

Advanced CCL17 Western Blot Tips

Deeper troubleshooting and optimisation questions for CCL17, answered from its protein features.

Which band should guide the blot?
Use 10.5 kDa, the observation attached to the authoritative PB9031 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 10.5 kDa expectation.
Which positive control should I start with?
Start with Cerebellum, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Soft tissue as an orthogonal HPA Not detected candidate.
Which gel should I use?
Use 15% consistently across the quick facts, protocol table, and poster.
What transfer method to use for CCL17 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PB9031 be started?
Start at the linked datasheet condition and run a three-point primary-antibody dilution test.
Which publication-derived protocols can I compare?
Compare only the supplied target-verified records: PMC6689663, PMC12020124, PMC5945007.
Boster reagents

CCL17 Western Blot Reagents

Mouse-reactive CCL17 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for CCL17 using PB9031; observed band 10.5 kDa
Anti-TARC/CCL17 Antibody Picoband®
Cat # PB9031
Reactivity: Mouse

Only image-backed, WB-validated Human/Mouse/Rat recommendations from the prepared catalog evidence are shown.

Source: prepared picoband-wb product evidence; each card retains its own SKU, URL, observed band, and authoritative WB image.