SPN · Western blot design guide

SPN Western Blot Planning Guide

Plan a SPN Western blot around the catalog-observed 40.3 kDa band, image-backed M01296-1 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 SPN: expected band 40.3 kDa, antibody M01296-1, and PMC-cited SDS-PAGE protocol steps
SPN Western blot protocol sheet — expected band 40.3 kDa, antibody M01296-1, controls and PMC citations. Open the full SPN WB guide →

SPN 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 40.3 kDa
Observed band Not reported — verify product WB image
Gel 12-15%
Positive control ⓘ Lung
Negative control ⓘ Bronchus
Important caveats
Reasons your observed band may differ from the expected size.
ⓘ Calculated mass 40.3 kDa
ⓘ Localization Membrane / Cell projection, microvillus
ⓘ Processing / PTM Record-dependent
ⓘ Reactivity Human / Mouse / Rat
Section 1

Real Curated SPN 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
PrimaryM01296-1 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 SPN Western Blot Band Size?

Use the product-observed 40.3 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
40.3 kDaMatches the authoritative product WB observation.
40.3 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected SPN appearancePlan around 40.3 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band40.3 kDa; use this as the primary experimental expectation.
Calculated mass40.3 kDa from UniProt P16150; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with M01296-1.
Why is my band missing or off?
SituationLikely causeNext action
40.3 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 SPN Western blot

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

HPA tissue expression evidence for SPN

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
Lung Reported tissue cells High Protein (HPA) HPA →
Skin Reported tissue cells High Protein (HPA) HPA →
Appendix Reported tissue cells High Protein (HPA) HPA →
Bone marrow Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

TissueCell typeLevelEvidenceSource
Bronchus Reported tissue cells Not detected Protein (HPA) HPA →
Caudate Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced SPN Western Blot Tips

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

Which band should guide the blot?
Use 40.3 kDa, the observation attached to the authoritative M01296-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 40.3 kDa expectation.
Which positive control should I start with?
Start with Lung, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Bronchus 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 SPN Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should M01296-1 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

SPN Western Blot Reagents

Human/Mouse/Rat-reactive SPN Western blot reagents with authoritative product imagery.

Real WB data Western blot validation image for SPN using M01296-1; observed band 40.3 kDa
Anti-CD43/SPN Antibody Picoband® (monoclonal, 4I3)
Cat # M01296-1
Real WB data Western blot validation image for SPN using PB9095; observed band 40.3 kDa
Anti-CD43/SPN Antibody Picoband®
Cat # PB9095

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 P16150
  2. Human Protein Atlas — SPN
  3. M01296-1 product record
  4. PMC2527098 — The cleavage of neutrophil leukosialin (CD43) by cathepsin G releases its extracellular domain and triggers its intramembrane proteolysis by presenilin/gamma-secretase (The Journal of biological chemistry, 2008)