FGF1 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 17.5 kDa observed
Observed band 17.5 kDa observed
Gel 15%
Positive control Kidney
Negative control Adipose tissue
Important caveats
Reasons your observed band may differ from the expected size.
Calculated mass17.5 kDa
LocalizationSecreted / Cytoplasm
Processing / PTMRecord-dependent
ReactivityHuman / Mouse / Rat
Section 1

Real Curated FGF1 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateKidney
Gel %15%
Load20-30 µg total protein per lane
TransferSemi-dry, short transfer
Membrane0.2 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryPB9241 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 FGF1 Western Blot Band Size?

Use the product-observed 17.5 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
17.5 kDaMatches the authoritative product WB observation.
17.5 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected FGF1 appearancePlan around 17.5 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band17.5 kDa; use this as the primary experimental expectation.
Calculated mass17.5 kDa from UniProt P05230; retain as context.
Gel selection15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PB9241.
Why is my band missing or off?
SituationLikely causeNext action
17.5 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 FGF1 Western blot

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

HPA tissue expression evidence for FGF1

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
Kidney Reported tissue cells High Protein (HPA) HPA →
Breast Reported tissue cells Low Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Adipose tissue Reported tissue cells Not detected Protein (HPA) HPA →
Adrenal gland Reported tissue cells Not detected Protein (HPA) HPA →
Appendix Reported tissue cells Not detected Protein (HPA) HPA →
Bone marrow Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced FGF1 Western Blot Tips

Deeper troubleshooting and optimisation questions for FGF1, answered from its protein features.

Which band should guide the blot?
Use 17.5 kDa, the observation attached to the authoritative PB9241 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 17.5 kDa expectation.
Which positive control should I start with?
Start with Kidney, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Adipose tissue as an orthogonal HPA Not detected candidate.
Which gel should I use?
Use 15% consistently across the quick facts, protocol table, and poster.
What transfer method to use for FGF1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PB9241 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

FGF1 Western Blot Reagents

Human/Mouse/Rat-reactive FGF1 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for FGF1 using PB9241; observed band 17.5 kDa
Anti-FGF1 Antibody Picoband®
Cat # PB9241
Real WB dataWestern blot validation image for FGF1 using PB9944; observed band 17.5 kDa
Anti-FGF1 Antibody Picoband®
Cat # PB9944
Real WB dataWestern blot validation image for FGF1 using RP1005; observed band 17.5 kDa
Anti-Fibroblast growth factor 1 FGF1 Antibody Picoband®
Cat # RP1005

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.