ATXN2 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 140.3 kDa observed
Observed band 140.3 kDa observed
Gel 8-10%
Positive control ⓘ Cerebellum
Negative control ⓘ Skeletal muscle
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass140.3 kDa
ⓘLocalizationCytoplasm
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman / Mouse / Rat
Section 1

Real Curated ATXN2 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateCaudate
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
PrimaryA01915 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 ATXN2 Western Blot Band Size?

Use the product-observed 140.3 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
140.3 kDaMatches the authoritative product WB observation.
140.3 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected ATXN2 appearancePlan around 140.3 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band140.3 kDa; use this as the primary experimental expectation.
Calculated mass140.3 kDa from UniProt Q99700; retain as context.
Gel selection8-10%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A01915.
Why is my band missing or off?
SituationLikely causeNext action
140.3 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 ATXN2 Western blot

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

HPA tissue expression evidence for ATXN2

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 →
Lung Reported tissue cells High Protein (HPA) HPA →
Gallbladder Reported tissue cells High Protein (HPA) HPA →
Caudate Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Skeletal muscle Reported tissue cells Not detected Protein (HPA) HPA →
Spleen Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced ATXN2 Western Blot Tips

Deeper troubleshooting and optimisation questions for ATXN2, answered from its protein features.

Which band should guide the blot?
Use 140.3 kDa, the observation attached to the authoritative A01915 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 140.3 kDa expectation.
Which positive control should I start with?
Start with Cerebellum, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Skeletal 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 ATXN2 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A01915 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

ATXN2 Western Blot Reagents

Human/Mouse/Rat-reactive ATXN2 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for ATXN2 using A01915; observed band 140.3 kDa
Anti-SCA2/ATXN2 Antibody Picoband®
Cat # A01915
Real WB dataWestern blot validation image for ATXN2 using PA2098; observed band 140.3 kDa
Anti-ATX2/ATXN2 Antibody Picoband®
Cat # PA2098
Real WB dataWestern blot validation image for ATXN2 using PB9483; observed band 140.3 kDa
Anti-ATX2/ATXN2 Antibody Picoband®
Cat # PB9483

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.