SMN1 · Western blot design guide

SMN1 Western Blot Planning Guide

Plan a SMN1 Western blot around the catalog-observed 31.8 kDa band, image-backed M03420-1 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 SMN1: expected band 31.8 kDa, antibody M03420-1, and PMC-cited SDS-PAGE protocol steps
SMN1 Western blot protocol sheet — expected band 31.8 kDa, antibody M03420-1, controls and PMC citations. Open the full SMN1 WB guide →

SMN1 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 31.8 kDa
Observed band Not reported — verify product WB image
Gel 12-15%
Positive control ⓘ Cerebellum
Negative control ⓘ Soft tissue
Important caveats
Reasons your observed band may differ from the expected size.
ⓘ Calculated mass 31.8 kDa
ⓘ Localization Nucleus, gem / Nucleus, Cajal body
ⓘ Processing / PTM Record-dependent
ⓘ Reactivity Human / Mouse / Rat
Section 1

Real Curated SMN1 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateBone marrow
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
PrimaryM03420-1 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 SMN1 Western Blot Band Size?

Use the product-observed 31.8 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
31.8 kDaMatches the authoritative product WB observation.
31.8 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected SMN1 appearancePlan around 31.8 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band31.8 kDa; use this as the primary experimental expectation.
Calculated mass31.8 kDa from UniProt Q16637; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with M03420-1.
Why is my band missing or off?
SituationLikely causeNext action
31.8 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 SMN1 Western blot

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

HPA tissue expression evidence for SMN1

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
Cerebellum Reported tissue cells High Protein (HPA) HPA →
Caudate Reported tissue cells High Protein (HPA) HPA →
Bone marrow Reported tissue cells High Protein (HPA) HPA →
Bronchus Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

TissueCell typeLevelEvidenceSource
Soft tissue Reported tissue cells Not detected Protein (HPA) HPA →
Liver Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced SMN1 Western Blot Tips

Deeper troubleshooting and optimisation questions for SMN1, answered from its protein features.

Which band should guide the blot?
Use 31.8 kDa, the observation attached to the authoritative M03420-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 31.8 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 12-15% consistently across the quick facts, protocol table, and poster.
What transfer method to use for SMN1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should M03420-1 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

SMN1 Western Blot Reagents

Human/Mouse/Rat-reactive SMN1 Western blot reagents with authoritative product imagery.

Real WB data Western blot validation image for SMN1 using M03420-1; observed band 31.8 kDa
Anti-SMN1/2 Antibody Picoband® (monoclonal, 2B10)
Cat # M03420-1
Real WB data Western blot validation image for SMN1 using PB9398; observed band 31.8 kDa
Anti-SMN1/2 Antibody Picoband®
Cat # PB9398

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 Q16637
  2. Human Protein Atlas — SMN1
  3. M03420-1 product record
  4. PMC4851398 — Enhanced snoMEN Vectors Facilitate Establishment of GFP-HIF-1α Protein Replacement Human Cell Lines (PloS one, 2016)
  5. PMC3636044 — Analysis of human protein replacement stable cell lines established using snoMEN-PR vector (PloS one, 2013)
  6. PMC8872419 — Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy (Genes, 2022)