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- Table of Contents
TRIP10 · Western blot design guide
TRIP10 Western Blot Planning Guide
Plan a TRIP10 Western blot around the catalog-observed 68.4 kDa band, image-backed A03963-1 evidence, HPA controls, and verified protocol records.
Evidence assembled July 2026 · For research use; verify linked source records and product datasheet before use
TRIP10 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 | 68.4 kDa | |
| Observed band | Not reported — verify product WB image | |
| Gel | 12-15% | |
| Positive control | Esophagus | |
| Negative control | Cerebral cortex |
Important caveats
Reasons your observed band may differ from the expected size.
| ⓘ | Calculated mass | 68.4 kDa |
| ⓘ | Localization | Cytoplasm, cytoskeleton / Cytoplasm, cell cortex |
| ⓘ | Processing / PTM | Record-dependent |
| ⓘ | Reactivity | Human / Rat |
Section 1
Real Curated TRIP10 Western Blot Protocols
Start with the molecular-weight rule, then compare verified publication-derived conditions.
| Sample / lysate | Appendix |
| Gel % | 12-15% |
| Load | 20-30 µg total protein per lane |
| Transfer | Semi-dry, standard transfer |
| Membrane | 0.45 µm PVDF |
| Blocking | 5% non-fat milk or 5% BSA in TBST |
| Primary | A03963-1 at datasheet starting dilution |
| Primary incubation | Overnight at 4 °C with gentle agitation |
| Secondary | Species-matched HRP conjugate at validated dilution |
| Wash | 3 × 5 min in TBST |
| Detection | Chemiluminescent substrate |
| Exposure | Bracket exposures to avoid saturation |
Section 2
What Is the Expected TRIP10 Western Blot Band Size?
Use the product-observed 68.4 kDa band as the primary planning value and retain the UniProt calculated mass as context.
| 68.4 kDa | Matches the authoritative product WB observation. |
| 68.4 kDa calculated | Use as UniProt context, not as a replacement observed band. |
| Unexpected additional signal | Do not assign identity without orthogonal positive/negative controls. |
💡Expected TRIP10 appearancePlan around 68.4 kDa and keep the calculated mass as supporting context.
| Catalog-observed band | 68.4 kDa; use this as the primary experimental expectation. |
| Calculated mass | 68.4 kDa from UniProt Q15642; retain as context. |
| Gel selection | 12-15%; shared with the recommended protocol and poster. |
| Specificity check | Compare the lead HPA positive and negative controls with A03963-1. |
| Situation | Likely cause | Next action |
|---|---|---|
| 68.4 kDa | Matches the authoritative product WB observation. | Confirm with orthogonal controls and the linked product record. |
| Additional band | May reflect processing, modification, or non-specific signal. | Run a dilution series and compare positive/negative controls. |
| Weak signal | Target abundance or transfer may be limiting. | Verify transfer, increase positive-control abundance, and bracket exposure. |
Experiment evidence
Western blot images showing TRIP10 band
A03963-1 · TRIP10
← swipe / scroll for more images →
Real WB data behind the band-size expectations in this section.
Sample controls for TRIP10 Western blot
🧪Use Esophagus as the first positive-control candidate and Cerebral cortex as the HPA Not detected negative candidate.
Positive control: Esophagus (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 TRIP10
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
| Tissue | Cell type | Level | Evidence | Source |
|---|---|---|---|---|
| Esophagus | Reported tissue cells | High | Protein (HPA) | HPA → |
| Colon | Reported tissue cells | High | Protein (HPA) | HPA → |
| Appendix | Reported tissue cells | High | Protein (HPA) | HPA → |
| Bronchus | Reported tissue cells | High | Protein (HPA) | HPA → |
Section 3
Advanced TRIP10 Western Blot Tips
Deeper troubleshooting and optimisation questions for TRIP10, answered from its protein features.
Which band should guide the blot?
Use 68.4 kDa, the observation attached to the authoritative A03963-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 68.4 kDa expectation.
Which positive control should I start with?
Start with Esophagus, 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 TRIP10 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A03963-1 be started?
Start at the linked datasheet condition and run a three-point primary-antibody dilution test.
Which publication-derived protocols can I compare?
Compare only the supplied target-verified records: PMC5150262, PMC5140099, PMC3044094.
Boster reagents
TRIP10 Western Blot Reagents
Human/Rat-reactive TRIP10 Western blot reagents with authoritative product imagery.
Real WB data
Anti-Cip4/TRIP10 Antibody Picoband®
Cat # A03963-1
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
- UniProt Q15642
- Human Protein Atlas — TRIP10
- A03963-1 product record
- PMC5150262 — Defining functional interactions during biogenesis of epithelial junctions.
- PMC5140099 — Alternative Splicing of Four Trafficking Genes Regulates Myofiber Structure and Skeletal Muscle Physiology.
- PMC3044094 — Functional characterization of Trip10 in cancer cell growth and survival.