NOS1 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 161 kDa observed
Observed band 161 kDa observed
Gel 8-10%
Positive control ⓘ Caudate
Negative control ⓘ Adipose tissue
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass161 kDa
ⓘLocalizationCell membrane, sarcolemma / Cell projection, dendritic spine
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman / Mouse / Rat
Section 1

Real Curated NOS1 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateCaudate
Gel %8-10%
Load20-30 µg total protein per lane
TransferWet/tank, extended transfer
Membrane0.45 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryA01070 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 NOS1 Western Blot Band Size?

Use the product-observed 161 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
161 kDaMatches the authoritative product WB observation.
161 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected NOS1 appearancePlan around 161 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band161 kDa; use this as the primary experimental expectation.
Calculated mass161 kDa from UniProt P29475; retain as context.
Gel selection8-10%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A01070.
Why is my band missing or off?
SituationLikely causeNext action
161 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 NOS1 Western blot

🧪Use Caudate as the first positive-control candidate and retain an orthogonal negative control.
Positive control: Caudate (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 NOS1

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 →
Cerebellum Reported tissue cells High Protein (HPA) HPA →
Hippocampus Reported tissue cells Medium Protein (HPA) HPA →
Kidney Reported tissue cells Medium 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 →
Section 3

Advanced NOS1 Western Blot Tips

Deeper troubleshooting and optimisation questions for NOS1, answered from its protein features.

Which band should guide the blot?
Use 161 kDa, the observation attached to the authoritative A01070 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 161 kDa expectation.
Which positive control should I start with?
Start with Caudate, 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 8-10% consistently across the quick facts, protocol table, and poster.
What transfer method to use for NOS1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A01070 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

NOS1 Western Blot Reagents

Human/Mouse/Rat-reactive NOS1 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for NOS1 using A01070; observed band 161 kDa
Anti-nNOS (neuronal)/NOS1 Antibody Picoband®
Cat # A01070
Real WB dataWestern blot validation image for NOS1 using A01070-2; observed band 161 kDa
Anti-nNOS (neuronal)/NOS1 Antibody Picoband®
Cat # A01070-2
Real WB dataWestern blot validation image for NOS1 using PA1329; observed band 161 kDa
Anti-nNOS (neuronal)/NOS1 Antibody Picoband®
Cat # PA1329

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.