ILK 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 51.4 kDa observed
Observed band 51.4 kDa observed
Gel 12-15%
Positive control Kidney
Negative control Cerebral cortex
Important caveats
Reasons your observed band may differ from the expected size.
Calculated mass51.4 kDa
LocalizationCell junction, focal adhesion / Cell membrane
Processing / PTMRecord-dependent
ReactivityHuman / Mouse / Rat
Section 1

Real Curated ILK Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateKidney
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
PrimaryA02932-3 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 2

What Is the Expected ILK Western Blot Band Size?

Use the product-observed 51.4 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
51.4 kDaMatches the authoritative product WB observation.
51.4 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected ILK appearancePlan around 51.4 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band51.4 kDa; use this as the primary experimental expectation.
Calculated mass51.4 kDa from UniProt Q13418; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A02932-3.
Why is my band missing or off?
SituationLikely causeNext action
51.4 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 ILK Western blot

🧪Use Kidney as the first positive-control candidate and retain an orthogonal negative control.
Positive control: Kidney (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 ILK

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
Kidney Reported tissue cells High Protein (HPA) HPA →
Skeletal muscle Reported tissue cells High Protein (HPA) HPA →
Adrenal gland Reported tissue cells Medium Protein (HPA) HPA →
Bone marrow Reported tissue cells Medium 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 ILK Western Blot Tips

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

Which band should guide the blot?
Use 51.4 kDa, the observation attached to the authoritative A02932-3 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 51.4 kDa expectation.
Which positive control should I start with?
Start with Kidney, 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 ILK Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A02932-3 be started?
Start at the linked datasheet condition and run a three-point primary-antibody dilution test.
Which publication-derived protocols can I compare?
No verified publication protocol was supplied; use only the deterministic recommended protocol.
Boster reagents

ILK Western Blot Reagents

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

Real WB dataWestern blot validation image for ILK using A02932-3; observed band 51.4 kDa
Anti-Integrin linked ILK Antibody Picoband®
Cat # A02932-3
Real WB dataWestern blot validation image for ILK using A02932-2; observed band 51.4 kDa
Anti-Integrin linked ILK Antibody Picoband®
Cat # A02932-2
Real WB dataWestern blot validation image for ILK using M02932-2; observed band 51.4 kDa
Anti-Integrin linked ILK Antibody Picoband® (monoclonal, 3C7E1)
Cat # M02932-2
Real WB dataWestern blot validation image for ILK using PB9949; observed band 51.4 kDa
Anti-Integrin linked ILK Antibody Picoband®
Cat # PB9949

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.