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- Table of Contents
FXR1 · Western blot design guide
FXR1 Western Blot Planning Guide
Plan a FXR1 Western blot around the catalog-observed 69.7 kDa band, image-backed A03308-2 evidence, HPA controls, and verified protocol records.
Evidence assembled July 2026 · For research use; verify linked source records and product datasheet before use
FXR1 Western Blot Experimental Design Guide
Expected bands, documented protocol parameters, controls and antibodies — the at-a-glance facts below, then the full design guide.
Must know before running
| Expected band | 69.7 kDa | |
| Observed band | Not reported — verify product WB image | |
| Gel | 12-15% | |
| Positive control | Adrenal gland | |
| Negative control | Soft tissue |
Important caveats
Reasons your observed band may differ from the expected size.
| ⓘ | Calculated mass | 69.7 kDa |
| ⓘ | Localization | Cytoplasm, Cytoplasmic ribonucleoprotein granule / Cytoplasm, Stress granule |
| ⓘ | Processing / PTM | Record-dependent |
| ⓘ | Reactivity | Human / Mouse / Rat |
Sample controls for FXR1 Western blot
🧪Use Adrenal gland as the first positive-control candidate and Soft tissue as the HPA Not detected negative candidate.
Positive control: Adrenal gland (High)
Negative control: Soft tissue (Not detected)
HPA protein score determines control status; other expression data is supporting context only.
HPA tissue expression evidence for FXR1
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 |
|---|---|---|---|---|
| Adrenal gland | Reported tissue cells | High | Protein (HPA) | HPA → |
| Breast | Reported tissue cells | High | Protein (HPA) | HPA → |
| Appendix | Reported tissue cells | High | Protein (HPA) | HPA → |
| Bone marrow | Reported tissue cells | High | Protein (HPA) | HPA → |
Section 1
What Is the Expected FXR1 Western Blot Band Size?
Use the product-observed 69.7 kDa band as the primary planning value and retain the UniProt calculated mass as context.
| 69.7 kDa | Matches the authoritative product WB observation. |
| 69.7 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 FXR1 appearancePlan around 69.7 kDa and keep the calculated mass as supporting context.
| Catalog-observed band | 69.7 kDa; use this as the primary experimental expectation. |
| Calculated mass | 69.7 kDa from UniProt P51114; 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 A03308-2. |
| Situation | Likely cause | Next action |
|---|---|---|
| 69.7 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 FXR1 band
A03308-2 · FXR1Observed 69.7 kDa · product-specific WB image
← swipe / scroll for more images →
Real WB data behind the band-size expectations in this section.
Section 2
Real Curated FXR1 Western Blot Protocols
Start with the molecular-weight rule, then compare verified publication-derived conditions.
| Sample / lysate | Adrenal gland |
| 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 | A03308-2 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 4
Advanced FXR1 Western Blot Tips
Deeper troubleshooting and optimisation questions for FXR1, answered from its protein features.
Which band should guide the blot?
Use 69.7 kDa, the observation attached to the authoritative A03308-2 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 69.7 kDa expectation.
Which positive control should I start with?
Start with Adrenal gland, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Soft tissue 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 FXR1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A03308-2 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: PMC7952250, PMC9616492, PMC11973456.
Boster reagents
FXR1 Western Blot Reagents
Human/Mouse/Rat-reactive FXR1 Western blot reagents with authoritative product imagery.
Real WB data
Anti-FXR1 Antibody Picoband®
Cat # A03308-2
Reactivity: Human, Mouse, Rat, Monkey
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 P51114
- Human Protein Atlas — FXR1
- A03308-2 product record
- PMC7952250 — circNRIP1 facilitates keloid progression via FXR1‑mediated upregulation of miR‑503‑3p and miR‑503‑5p.
- PMC9616492 — Ribosome changes reprogram translation for chemosurvival in G0 leukemic cells.
- PMC11973456 — Estrogen-induced FXR1 promotes endocrine resistance and bone metastasis in breast cancer via BCL2 and GPX4.