CD46 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 43.7 kDa observed
Observed band 43.7 kDa observed
Gel 12-15%
Positive control ⓘ Breast
Negative control ⓘ Cerebral cortex
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass43.7 kDa
ⓘLocalizationCytoplasmic vesicle, secretory vesicle, acrosome inner membrane
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman / Mouse / Rat
Section 1

Real Curated CD46 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateBreast
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
PrimaryM00377-2 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 CD46 Western Blot Band Size?

Use the product-observed 43.7 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
43.7 kDaMatches the authoritative product WB observation.
43.7 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected CD46 appearancePlan around 43.7 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band43.7 kDa; use this as the primary experimental expectation.
Calculated mass43.7 kDa from UniProt P15529; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with M00377-2.
Why is my band missing or off?
SituationLikely causeNext action
43.7 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 CD46 Western blot

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

HPA tissue expression evidence for CD46

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
Breast Reported tissue cells High Protein (HPA) HPA →
Gallbladder Reported tissue cells High Protein (HPA) HPA →
Colon 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
Cerebral cortex Reported tissue cells Not detected Protein (HPA) HPA →
Caudate Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced CD46 Western Blot Tips

Deeper troubleshooting and optimisation questions for CD46, answered from its protein features.

Which band should guide the blot?
Use 43.7 kDa, the observation attached to the authoritative M00377-2 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 43.7 kDa expectation.
Which positive control should I start with?
Start with Breast, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Cerebral cortex 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 CD46 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should M00377-2 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

CD46 Western Blot Reagents

Human/Mouse/Rat-reactive CD46 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for CD46 using M00377-2; observed band 43.7 kDa
Anti-CD46 Antibody Picoband® (monoclonal, 9E9)
Cat # M00377-2

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.