BCAR3 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 92.6 kDa
Observed band Not reported — verify product WB image
Gel 8-10%
Positive control ⓘ Cerebral cortex
Negative control ⓘ Oral mucosa
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass92.6 kDa
ⓘLocalizationCytoplasm / Cell junction, focal adhesion
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman / Mouse / Rat

Sample controls for BCAR3 Western blot

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

HPA tissue expression evidence for BCAR3

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
Cerebral cortex Reported tissue cells High Protein (HPA) HPA →
Breast Reported tissue cells Medium Protein (HPA) HPA →
Adrenal gland Reported tissue cells Medium Protein (HPA) HPA →
Endometrium Reported tissue cells Medium Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Oral mucosa Reported tissue cells Not detected Protein (HPA) HPA →
Ovary Reported tissue cells Not detected Protein (HPA) HPA →
Section 1

What Is the Expected BCAR3 Western Blot Band Size?

Use the product-observed 92.6 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
92.6 kDaMatches the authoritative product WB observation.
92.6 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected BCAR3 appearancePlan around 92.6 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band92.6 kDa; use this as the primary experimental expectation.
Calculated mass92.6 kDa from UniProt O75815; retain as context.
Gel selection8-10%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PB9846.
Why is my band missing or off?
SituationLikely causeNext action
92.6 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.
Section 2

Real Curated BCAR3 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateCerebral cortex
Gel %8-10%
Load20-30 µg total protein per lane
TransferSemi-dry, standard transfer
Membrane0.45 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryPB9846 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 4

Advanced BCAR3 Western Blot Tips

Deeper troubleshooting and optimisation questions for BCAR3, answered from its protein features.

Which band should guide the blot?
Use 92.6 kDa, the observation attached to the authoritative PB9846 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 92.6 kDa expectation.
Which positive control should I start with?
Start with Cerebral cortex, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Oral mucosa as an orthogonal HPA Not detected candidate.
Which gel should I use?
Use 8-10% consistently across the quick facts, protocol table, and poster.
What transfer method to use for BCAR3 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PB9846 be started?
Start at the linked datasheet condition and run a three-point primary-antibody dilution test.
Which publication-derived protocols can I compare?
Compare only the supplied target-verified records: PMC10898485, PMC2740797, PMC4311507.
Boster reagents

BCAR3 Western Blot Reagents

Human/Mouse/Rat-reactive BCAR3 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for BCAR3 using PB9846; observed band 92.6 kDa
Anti-BCAR3 Antibody Picoband®
Cat # PB9846
Reactivity: Human, Mouse, Rat

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.