ITGB2 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 84.8 kDa observed
Observed band 84.8 kDa observed
Gel 8-10%
Positive control Lung
Negative control Bronchus
Important caveats
Reasons your observed band may differ from the expected size.
Calculated mass84.8 kDa
LocalizationCell membrane / Membrane raft
Processing / PTMRecord-dependent
ReactivityHuman
Section 1

Real Curated ITGB2 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateAppendix
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
PrimaryM00458-1 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 ITGB2 Western Blot Band Size?

Use the product-observed 84.8 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
84.8 kDaMatches the authoritative product WB observation.
84.8 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected ITGB2 appearancePlan around 84.8 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band84.8 kDa; use this as the primary experimental expectation.
Calculated mass84.8 kDa from UniProt P05107; retain as context.
Gel selection8-10%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with M00458-1.
Why is my band missing or off?
SituationLikely causeNext action
84.8 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 ITGB2 Western blot

🧪Use Lung as the first positive-control candidate and retain an orthogonal negative control.
Positive control: Lung (High)
Negative control: Bronchus (Not detected)
HPA protein score determines control status; other expression data is supporting context only.

HPA tissue expression evidence for ITGB2

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
Lung Reported tissue cells High Protein (HPA) HPA →
Cerebellum Reported tissue cells High Protein (HPA) HPA →
Appendix Reported tissue cells High Protein (HPA) HPA →
Bone marrow Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Bronchus Reported tissue cells Not detected Protein (HPA) HPA →
Colon Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced ITGB2 Western Blot Tips

Deeper troubleshooting and optimisation questions for ITGB2, answered from its protein features.

Which band should guide the blot?
Use 84.8 kDa, the observation attached to the authoritative M00458-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 84.8 kDa expectation.
Which positive control should I start with?
Start with Lung, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Bronchus 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 ITGB2 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should M00458-1 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

ITGB2 Western Blot Reagents

Human-reactive ITGB2 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for ITGB2 using M00458-1; observed band 84.8 kDa
Anti-CD18 ITGB2 Antibody Picoband® (monoclonal, 1A3/2A10)
Cat # M00458-1
Real WB dataWestern blot validation image for ITGB2 using PA1623; observed band 84.8 kDa
Anti-CD18/ITGB2 Antibody Picoband®
Cat # PA1623
Real WB dataWestern blot validation image for ITGB2 using PB9141; observed band 84.8 kDa
Anti-CD18/ITGB2 Antibody Picoband®
Cat # PB9141

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.