This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
IFNGR1 · Western blot design guide
IFNGR1 Western Blot Planning Guide
Plan a IFNGR1 Western blot around the catalog-observed 54.4 kDa band, image-backed A01716-1 evidence, HPA controls, and verified protocol records.
Evidence assembled July 2026 · For research use; verify linked source records and product datasheet before use
IFNGR1 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 | 54.4 kDa observed | |
| Observed band | 54.4 kDa observed | |
| Gel | 12-15% | |
| Positive control | Caudate | |
| Negative control | Heart muscle |
Important caveats
Reasons your observed band may differ from the expected size.
| ⓘ | Calculated mass | 54.4 kDa |
| ⓘ | Localization | Cell membrane |
| ⓘ | Processing / PTM | Record-dependent |
| ⓘ | Reactivity | Human |
Section 1
Real Curated IFNGR1 Western Blot Protocols
Start with the molecular-weight rule, then compare verified publication-derived conditions.
| Sample / lysate | Caudate |
| 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 | A01716-1 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 IFNGR1 Western Blot Band Size?
Use the product-observed 54.4 kDa band as the primary planning value and retain the UniProt calculated mass as context.
| 54.4 kDa | Matches the authoritative product WB observation. |
| 54.4 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 IFNGR1 appearancePlan around 54.4 kDa and keep the calculated mass as supporting context.
| Catalog-observed band | 54.4 kDa; use this as the primary experimental expectation. |
| Calculated mass | 54.4 kDa from UniProt P15260; 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 A01716-1. |
| Situation | Likely cause | Next action |
|---|---|---|
| 54.4 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 IFNGR1 band
A01716-1 · IFNGR1Observed 54.4 kDa · product-specific WB image
← swipe / scroll for more images →
Real WB data behind the band-size expectations in this section.
Sample controls for IFNGR1 Western blot
🧪Use Caudate as the first positive-control candidate and retain an orthogonal negative control.
Positive control: Caudate (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 IFNGR1
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 |
|---|---|---|---|---|
| Caudate | Reported tissue cells | High | Protein (HPA) | HPA → |
| Cerebral cortex | Reported tissue cells | High | Protein (HPA) | HPA → |
| Duodenum | Reported tissue cells | High | Protein (HPA) | HPA → |
| Endometrium | Reported tissue cells | High | Protein (HPA) | HPA → |
Section 3
Advanced IFNGR1 Western Blot Tips
Deeper troubleshooting and optimisation questions for IFNGR1, answered from its protein features.
Which band should guide the blot?
Use 54.4 kDa, the observation attached to the authoritative A01716-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 54.4 kDa expectation.
Which positive control should I start with?
Start with Caudate, 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 IFNGR1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A01716-1 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
IFNGR1 Western Blot Reagents
Human-reactive IFNGR1 Western blot reagents with authoritative product imagery.
Real WB data
Anti-IFNGR1 Antibody Picoband®
Cat # A01716-1
Real WB data
Anti-IFNGR1 Antibody Picoband®
Cat # A01716-2
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.