EPCAM Western Blot Experimental Design Guide

Expected bands, validated protocols, controls and antibodies — the at-a-glance facts below, then the full design guide.

Must know before running
Expected band 34.9 kDa observed
Observed band 34.9 kDa observed
Gel 12-15%
Positive control Colon
Negative control Bone marrow
Important caveats
Reasons your observed band may differ from the expected size.
Calculated mass34.9 kDa
LocalizationLateral cell membrane / Cell junction, tight junction
Processing / PTMRecord-dependent
ReactivityHuman
Section 1

Real Curated EPCAM Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateAppendix
Gel %12-15%
Load20-30 µg total protein per lane
TransferSemi-dry, standard transfer
Membrane0.45 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryPB10059 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 2

What Is the Expected EPCAM Western Blot Band Size?

Use the product-observed 34.9 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
34.9 kDaMatches the authoritative product WB observation.
34.9 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected EPCAM appearancePlan around 34.9 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band34.9 kDa; use this as the primary experimental expectation.
Calculated mass34.9 kDa from UniProt P16422; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PB10059.
Why is my band missing or off?
SituationLikely causeNext action
34.9 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.

Sample controls for EPCAM Western blot

🧪Use Colon as the first positive-control candidate and retain an orthogonal negative control.
Positive control: Colon (High)
Negative control: Bone marrow (Not detected)
HPA protein score determines control status; other expression data is supporting context only.

HPA tissue expression evidence for EPCAM

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
Colon Reported tissue cells High Protein (HPA) HPA →
Fallopian tube Reported tissue cells High Protein (HPA) HPA →
Appendix Reported tissue cells High Protein (HPA) HPA →
Duodenum Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Bone marrow Reported tissue cells Not detected Protein (HPA) HPA →
Adipose tissue Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced EPCAM Western Blot Tips

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

Which band should guide the blot?
Use 34.9 kDa, the observation attached to the authoritative PB10059 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 34.9 kDa expectation.
Which positive control should I start with?
Start with Colon, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Bone marrow as an orthogonal HPA Not detected candidate.
Which gel should I use?
Use 12-15% consistently across the quick facts, protocol table, and poster.
What transfer method to use for EPCAM Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PB10059 be started?
Start at the linked datasheet condition and run a three-point primary-antibody dilution test.
Which publication-derived protocols can I compare?
No verified publication protocol was supplied; use only the deterministic recommended protocol.
Boster reagents

EPCAM Western Blot Reagents

Human-reactive EPCAM Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for EPCAM using PB10059; observed band 34.9 kDa
Anti-EpCAM Antibody Picoband®
Cat # PB10059

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.