WNT2B 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 43.8 kDa observed
Observed band 43.8 kDa observed
Gel 12-15%
Positive control ⓘ No defensible HPA tissue; use knockout/knockdown
Negative control ⓘ Use knockout/knockdown or orthogonal negative
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass43.8 kDa
ⓘLocalizationSecreted, extracellular space, extracellular matrix / Secreted
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman / Mouse / Rat
Section 1

Real Curated WNT2B Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateKnown-positive human lysate
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
PrimaryA04879-1 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 WNT2B Western Blot Band Size?

Use the product-observed 43.8 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
43.8 kDaMatches the authoritative product WB observation.
43.8 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected WNT2B appearancePlan around 43.8 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band43.8 kDa; use this as the primary experimental expectation.
Calculated mass43.8 kDa from UniProt Q93097; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A04879-1.
Why is my band missing or off?
SituationLikely causeNext action
43.8 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 WNT2B Western blot

🧪No defensible HPA positive control was available; do not invent one.
HPA protein score determines control status; other expression data is supporting context only.

HPA tissue expression evidence for WNT2B

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

Undetected expression · recommended negative controls

The Human Protein Atlas exposes no structured IHC tissue profile for WNT2B, so tissue-level positive/negative controls cannot be listed here. Use a documented WNT2B-positive lysate (recombinant WNT2B or a known-expressing line) as the positive control and a WNT2B knockdown/knockout lysate as the negative control; confirm against the antibody datasheet.
Tissue Cell type Level Evidence Source
Section 3

Advanced WNT2B Western Blot Tips

Deeper troubleshooting and optimisation questions for WNT2B, answered from its protein features.

Which band should guide the blot?
Use 43.8 kDa, the observation attached to the authoritative A04879-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 43.8 kDa expectation.
Which positive control should I start with?
No defensible positive tissue was supplied; do not invent one.
Which negative control is defensible?
Use a target knockdown/knockout control when no HPA Not detected tissue is available.
Which gel should I use?
Use 12-15% consistently across the quick facts, protocol table, and poster.
What transfer method to use for WNT2B Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A04879-1 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

WNT2B Western Blot Reagents

Human/Mouse/Rat-reactive WNT2B Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for WNT2B using A04879-1; observed band 43.8 kDa
Anti-Wnt2b Antibody Picoband®
Cat # A04879-1
Real WB dataWestern blot validation image for WNT2B using PA1985; observed band 43.8 kDa
Anti-Protein Wnt-2b Wnt2b Antibody Picoband®
Cat # PA1985
Real WB dataWestern blot validation image for WNT2B using PB9462; observed band 43.8 kDa
Anti-Wnt2b Antibody Picoband®
Cat # PB9462

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.