TUBB1 · Western blot design guide

TUBB1 Western Blot Planning Guide

Plan a TUBB1 Western blot around the catalog-observed 50.3 kDa band, image-backed A05397-1 evidence, HPA controls, and verified protocol records.

Evidence assembled July 2026 · For research use; verify linked source records and product datasheet before use
Western blot protocol sheet for TUBB1 (TUBB1): expected band 50.3 kDa, antibody A05397-1, and guide-derived SDS-PAGE protocol steps
TUBB1 Western blot protocol sheet — expected band 50.3 kDa, antibody A05397-1, controls and PMC citations. Open the full TUBB1 WB guide →

TUBB1 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 50.3 kDa
Observed band Not reported — verify product WB image
Gel 12-15%
Positive control ⓘ Testis
Negative control ⓘ Heart muscle
Important caveats
Reasons your observed band may differ from the expected size.
ⓘ Calculated mass 50.3 kDa
ⓘ Localization Cytoplasm, cytoskeleton
ⓘ Processing / PTM Record-dependent
ⓘ Reactivity Human / Mouse / Rat
Section 1

Real Curated TUBB1 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateTestis
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
PrimaryA05397-1 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 TUBB1 Western Blot Band Size?

Use the product-observed 50.3 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
50.3 kDaMatches the authoritative product WB observation.
50.3 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected TUBB1 appearancePlan around 50.3 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band50.3 kDa; use this as the primary experimental expectation.
Calculated mass50.3 kDa from UniProt Q9H4B7; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A05397-1.
Why is my band missing or off?
SituationLikely causeNext action
50.3 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 TUBB1 Western blot

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

HPA tissue expression evidence for TUBB1

Comprehensive Human Protein Atlas IHC scoring per tissue. Rows are taken directly from the HPA tissue chart — click any row's HPA link to view the source.

Positive expression · recommended positive controls

TissueCell typeLevelEvidenceSource
Testis Reported tissue cells High Protein (HPA) HPA →
Breast Reported tissue cells Medium Protein (HPA) HPA →
Adrenal gland Reported tissue cells Medium Protein (HPA) HPA →
Appendix Reported tissue cells Medium Protein (HPA) HPA →

Undetected expression · recommended negative controls

TissueCell typeLevelEvidenceSource
Heart muscle Reported tissue cells Not detected Protein (HPA) HPA →
Skeletal muscle Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced TUBB1 Western Blot Tips

Deeper troubleshooting and optimisation questions for TUBB1, answered from its protein features.

Which band should guide the blot?
Use 50.3 kDa, the observation attached to the authoritative A05397-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 50.3 kDa expectation.
Which positive control should I start with?
Start with Testis, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Heart muscle 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 TUBB1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A05397-1 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

TUBB1 Western Blot Reagents

Human/Mouse/Rat-reactive TUBB1 Western blot reagents with authoritative product imagery.

Real WB data Western blot validation image for TUBB1 using A05397-1; observed band 50.3 kDa
Anti-Tubulin beta Antibody Picoband®
Cat # A05397-1

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.

References

  1. UniProt Q9H4B7
  2. Human Protein Atlas — TUBB1
  3. A05397-1 product record
  4. PMC8203157 — Identification of novel TUBB1 variants in patients with macrothrombocytopenia (Turkish journal of medical sciences, 2021)
  5. PMC12927553 — Biogenesis and migration of the sperm cytoplasmic droplet require ARRDC5 and TEX38 (Cell reports, 2026)
  6. PMC4790753 — Bruton's tyrosine kinase revealed as a negative regulator of Wnt-beta-catenin signaling (Science signaling, 2009)