LIG3 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 112.9 kDa
Observed band Not reported — verify product WB image
Gel 8-10%
Positive control Cerebellum
Negative control Smooth muscle
Important caveats
Reasons your observed band may differ from the expected size.
Calculated mass112.9 kDa
LocalizationMitochondrion / Mitochondrion
Processing / PTMRecord-dependent
ReactivityHuman / Mouse / Rat

Sample controls for LIG3 Western blot

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

HPA tissue expression evidence for LIG3

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
Cerebellum Reported tissue cells High Protein (HPA) HPA →
Breast Reported tissue cells High Protein (HPA) HPA →
Bone marrow Reported tissue cells High Protein (HPA) HPA →
Bronchus Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Smooth muscle Reported tissue cells Not detected Protein (HPA) HPA →
Liver Reported tissue cells Not detected Protein (HPA) HPA →
Section 1

What Is the Expected LIG3 Western Blot Band Size?

Use the product-observed 112.9 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
112.9 kDaMatches the authoritative product WB observation.
112.9 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected LIG3 appearancePlan around 112.9 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band112.9 kDa; use this as the primary experimental expectation.
Calculated mass112.9 kDa from UniProt P49916; retain as context.
Gel selection8-10%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A02741-2.
Why is my band missing or off?
SituationLikely causeNext action
112.9 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 LIG3 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateBone marrow
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
PrimaryA02741-2 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 LIG3 Western Blot Tips

Deeper troubleshooting and optimisation questions for LIG3, answered from its protein features.

Which band should guide the blot?
Use 112.9 kDa, the observation attached to the authoritative A02741-2 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 112.9 kDa expectation.
Which positive control should I start with?
Start with Cerebellum, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Smooth muscle 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 LIG3 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A02741-2 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: PMC10363431, PMC6365379, PMC8241731.
Boster reagents

LIG3 Western Blot Reagents

Human/Mouse/Rat-reactive LIG3 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for LIG3 using A02741-2; observed band 112.9 kDa
Anti-DNA Ligase III/LIG3 Antibody Picoband®
Cat # A02741-2
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.