NME1 · Western blot design guide

NME1 Western Blot Planning Guide

Plan a NME1 Western blot around the catalog-observed 17.1 kDa band, image-backed PA1829 evidence, HPA controls, and verified protocol records.

Evidence assembled July 2026 · For research use; verify linked source records and product datasheet before use
Western blot protocol sheet for NME1 (NME1): expected band 17.1 kDa, antibody PA1829, and PMC-cited SDS-PAGE protocol steps
NME1 Western blot protocol sheet — expected band 17.1 kDa, antibody PA1829, controls and PMC citations. Open the full NME1 WB guide →

NME1 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 17.1 kDa
Observed band Not reported — verify product WB image
Gel 15%
Positive control ⓘ Breast
Negative control ⓘ Heart muscle
Important caveats
Reasons your observed band may differ from the expected size.
ⓘ Calculated mass 17.1 kDa
ⓘ Localization Cytoplasm / Nucleus
ⓘ Processing / PTM Record-dependent
ⓘ Reactivity Human / Mouse / Rat
Section 1

Real Curated NME1 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateBreast
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
PrimaryPA1829 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 NME1 Western Blot Band Size?

Use the product-observed 17.1 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
17.1 kDaMatches the authoritative product WB observation.
17.1 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected NME1 appearancePlan around 17.1 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band17.1 kDa; use this as the primary experimental expectation.
Calculated mass17.1 kDa from UniProt P15531; retain as context.
Gel selection15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PA1829.
Why is my band missing or off?
SituationLikely causeNext action
17.1 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 NME1 Western blot

🧪Use Breast as the first positive-control candidate and Heart muscle as the HPA Not detected negative candidate.
Positive control: Breast (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 NME1

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

TissueCell typeLevelEvidenceSource
Breast Reported tissue cells High Protein (HPA) HPA →
Endometrium Reported tissue cells High Protein (HPA) HPA →
Lymph node Reported tissue cells High Protein (HPA) HPA →
Adrenal gland Reported tissue cells Medium Protein (HPA) HPA →

Undetected expression · recommended negative controls

TissueCell typeLevelEvidenceSource
Heart muscle Reported tissue cells Not detected Protein (HPA) HPA →
Skeletal muscle Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced NME1 Western Blot Tips

Deeper troubleshooting and optimisation questions for NME1, answered from its protein features.

Which band should guide the blot?
Use 17.1 kDa, the observation attached to the authoritative PA1829 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 17.1 kDa expectation.
Which positive control should I start with?
Start with Breast, 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 15% consistently across the quick facts, protocol table, and poster.
What transfer method to use for NME1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PA1829 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: PMC8212152, PMC8195739, PMC6115381.
Boster reagents

NME1 Western Blot Reagents

Human/Mouse/Rat-reactive NME1 Western blot reagents with authoritative product imagery.

Real WB data Western blot validation image for NME1 using PA1829; observed band 17.1 kDa
Anti-NM23A/NME1 Antibody Picoband®
Cat # PA1829
Real WB data Western blot validation image for NME1 using RP1090; observed band 17.1 kDa
Anti-NM23A/NME1 Antibody Picoband®
Cat # RP1090

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.