GATA6 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 60 kDa
Observed band Not reported — verify product WB image
Gel 12-15%
Positive control ⓘ Gallbladder
Negative control ⓘ Cerebral cortex
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass60 kDa
ⓘLocalizationNucleus
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman

Sample controls for GATA6 Western blot

🧪Use Gallbladder as the first positive-control candidate and Cerebral cortex as the HPA Not detected negative candidate.
Positive control: Gallbladder (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 GATA6

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
Gallbladder Reported tissue cells High Protein (HPA) HPA →
Pancreas 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 →
Heart muscle Reported tissue cells Not detected Protein (HPA) HPA →
Section 1

What Is the Expected GATA6 Western Blot Band Size?

Use the product-observed 60 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
60 kDaMatches the authoritative product WB observation.
60 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected GATA6 appearancePlan around 60 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band60 kDa; use this as the primary experimental expectation.
Calculated mass60 kDa from UniProt Q92908; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A00778-3.
Why is my band missing or off?
SituationLikely causeNext action
60 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 GATA6 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateColon
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
PrimaryA00778-3 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 GATA6 Western Blot Tips

Deeper troubleshooting and optimisation questions for GATA6, answered from its protein features.

Which band should guide the blot?
Use 60 kDa, the observation attached to the authoritative A00778-3 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 60 kDa expectation.
Which positive control should I start with?
Start with Gallbladder, 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 GATA6 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A00778-3 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: PMC5354868, PMC9118154.
Boster reagents

GATA6 Western Blot Reagents

Human-reactive GATA6 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for GATA6 using A00778-3; observed band 60 kDa
Anti-GATA6 Antibody Picoband®
Cat # A00778-3
Reactivity: Human

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.