EIF2AK4 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 186.9 kDa observed
Observed band 186.9 kDa observed
Gel 8-10%
Positive control Cerebral cortex
Negative control Duodenum
Important caveats
Reasons your observed band may differ from the expected size.
Calculated mass186.9 kDa
LocalizationCytoplasm
Processing / PTMRecord-dependent
ReactivityHuman / Mouse / Rat
Section 1

Real Curated EIF2AK4 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateCerebral cortex
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
PrimaryA01172-2 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 EIF2AK4 Western Blot Band Size?

Use the product-observed 186.9 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
186.9 kDaMatches the authoritative product WB observation.
186.9 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected EIF2AK4 appearancePlan around 186.9 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band186.9 kDa; use this as the primary experimental expectation.
Calculated mass186.9 kDa from UniProt Q9P2K8; retain as context.
Gel selection8-10%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A01172-2.
Why is my band missing or off?
SituationLikely causeNext action
186.9 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 EIF2AK4 Western blot

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

HPA tissue expression evidence for EIF2AK4

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
Cerebral cortex Reported tissue cells High Protein (HPA) HPA →
Lymph node Reported tissue cells High Protein (HPA) HPA →
Placenta Reported tissue cells High Protein (HPA) HPA →
Adrenal gland Reported tissue cells Medium Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Duodenum Reported tissue cells Not detected Protein (HPA) HPA →
Oral mucosa Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced EIF2AK4 Western Blot Tips

Deeper troubleshooting and optimisation questions for EIF2AK4, answered from its protein features.

Which band should guide the blot?
Use 186.9 kDa, the observation attached to the authoritative A01172-2 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 186.9 kDa expectation.
Which positive control should I start with?
Start with Cerebral cortex, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Duodenum 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 EIF2AK4 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A01172-2 be started?
Start at the linked datasheet condition and run a three-point primary-antibody dilution test.
Which publication-derived protocols can I compare?
No verified publication protocol was supplied; use only the deterministic recommended protocol.
Boster reagents

EIF2AK4 Western Blot Reagents

Human/Mouse/Rat-reactive EIF2AK4 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for EIF2AK4 using A01172-2; observed band 186.9 kDa
Anti-EIF2AK4 Antibody Picoband®
Cat # A01172-2
Real WB dataWestern blot validation image for EIF2AK4 using PA2028; observed band 186.9 kDa
Anti-GCN2/EIF2AK4 Antibody Picoband®
Cat # PA2028

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.