PROCR · Western blot design guide

PROCR Western Blot Planning Guide

Plan a PROCR Western blot around the catalog-observed 26.7 kDa band, image-backed PB9880 evidence, HPA controls, and verified protocol records.

Evidence assembled July 2026 · For research use; verify linked source records and product datasheet before use
Western blot protocol sheet for PROCR (PROCR): expected band 26.7 kDa, antibody PB9880, and guide-derived SDS-PAGE protocol steps
PROCR Western blot protocol sheet — expected band 26.7 kDa, antibody PB9880, controls and PMC citations. Open the full PROCR WB guide →

PROCR 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 26.7 kDa
Observed band Not reported — verify product WB image
Gel 12-15%
Positive control ⓘ Rectum
Negative control ⓘ Appendix
Important caveats
Reasons your observed band may differ from the expected size.
ⓘ Calculated mass 26.7 kDa
ⓘ Localization Membrane
ⓘ Processing / PTM Record-dependent
ⓘ Reactivity Human
Section 1

Real Curated PROCR Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateRectum
Gel %12-15%
Load20-30 µg total protein per lane
TransferSemi-dry, short transfer
Membrane0.45 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryPB9880 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 PROCR Western Blot Band Size?

Use the product-observed 26.7 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
26.7 kDaMatches the authoritative product WB observation.
26.7 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected PROCR appearancePlan around 26.7 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band26.7 kDa; use this as the primary experimental expectation.
Calculated mass26.7 kDa from UniProt Q9UNN8; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PB9880.
Why is my band missing or off?
SituationLikely causeNext action
26.7 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 PROCR Western blot

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

HPA tissue expression evidence for PROCR

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

Positive expression · recommended positive controls

TissueCell typeLevelEvidenceSource
Rectum Reported tissue cells High Protein (HPA) HPA →
Kidney Reported tissue cells Medium Protein (HPA) HPA →
Bronchus Reported tissue cells Medium Protein (HPA) HPA →
Caudate Reported tissue cells Low Protein (HPA) HPA →

Undetected expression · recommended negative controls

TissueCell typeLevelEvidenceSource
Appendix Reported tissue cells Not detected Protein (HPA) HPA →
Cerebellum Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced PROCR Western Blot Tips

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

Which band should guide the blot?
Use 26.7 kDa, the observation attached to the authoritative PB9880 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 26.7 kDa expectation.
Which positive control should I start with?
Start with Rectum, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Appendix 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 PROCR Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PB9880 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

PROCR Western Blot Reagents

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

Real WB data Western blot validation image for PROCR using PB9880; observed band 26.7 kDa
Anti-EPCR/CD201/PROCR Antibody Picoband®
Cat # PB9880

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.

References

  1. UniProt Q9UNN8
  2. Human Protein Atlas — PROCR
  3. PB9880 product record
  4. PMC12102113 — Human endothelial colony forming cells (ECFCs) require endothelial protein C receptor (EPCR) for cell cycle progression and angiogenic activity (Angiogenesis, 2025)
  5. PMC12322016 — PROCR diminishes the efficacy of radiation by impairing T-cell-mediated antitumour immunity (Nature communications, 2025)
  6. PMC8290623 — Lentiviral CRISPR-guided RNA library screening identified Adam17 as an upstream negative regulator of Procr in mammary epithelium (BMC biotechnology, 2021)