ITGA7 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 128.9 kDa
Observed band Not reported — verify product WB image
Gel 8-10%
Positive control ⓘ Adipose tissue
Negative control ⓘ Endometrium
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass128.9 kDa
ⓘLocalizationMembrane
ⓘProcessing / PTMRecord-dependent
ⓘReactivityRat / Mouse / Human

Sample controls for ITGA7 Western blot

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

HPA tissue expression evidence for ITGA7

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
Adipose tissue Reported tissue cells Medium Protein (HPA) HPA →
Breast Reported tissue cells Medium Protein (HPA) HPA →
Bone marrow Reported tissue cells Medium Protein (HPA) HPA →
Bronchus Reported tissue cells Medium Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Endometrium Reported tissue cells Not detected Protein (HPA) HPA →
Hippocampus Reported tissue cells Not detected Protein (HPA) HPA →
Section 1

What Is the Expected ITGA7 Western Blot Band Size?

Use the product-observed 128.9 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
128.9 kDaMatches the authoritative product WB observation.
128.9 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected ITGA7 appearancePlan around 128.9 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band128.9 kDa; use this as the primary experimental expectation.
Calculated mass128.9 kDa from UniProt Q13683; retain as context.
Gel selection8-10%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PA2226.
Why is my band missing or off?
SituationLikely causeNext action
128.9 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 ITGA7 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateAdipose tissue
Gel %8-10%
Load20-30 µg total protein per lane
TransferWet/tank, extended transfer
Membrane0.45 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryPA2226 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 ITGA7 Western Blot Tips

Deeper troubleshooting and optimisation questions for ITGA7, answered from its protein features.

Which band should guide the blot?
Use 128.9 kDa, the observation attached to the authoritative PA2226 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 128.9 kDa expectation.
Which positive control should I start with?
Start with Adipose tissue, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Endometrium 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 ITGA7 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PA2226 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: PMC8657770, PMC9143933, PMC9713827.
Boster reagents

ITGA7 Western Blot Reagents

Rat/Mouse/Human-reactive ITGA7 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for ITGA7 using PA2226; observed band 128.9 kDa
Anti-Integrin alpha-7 ITGA7 Antibody Picoband®
Cat # PA2226
Reactivity: Rat, Mouse, 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.