HTR1A 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 46.1 kDa
Observed band Not reported — verify product WB image
Gel 12-15%
Positive control ⓘ Cerebellum
Negative control ⓘ Bone marrow
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass46.1 kDa
ⓘLocalizationCell membrane / Cell projection, dendrite
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman / Rat

Sample controls for HTR1A Western blot

🧪Use Cerebellum as the first positive-control candidate and Bone marrow as the HPA Not detected negative candidate.
Positive control: Cerebellum (High)
Negative control: Bone marrow (Not detected)
HPA protein score determines control status; other expression data is supporting context only.

HPA tissue expression evidence for HTR1A

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
Cerebellum Reported tissue cells High Protein (HPA) HPA →
Colon Reported tissue cells High Protein (HPA) HPA →
Duodenum Reported tissue cells High Protein (HPA) HPA →
Kidney Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Bone marrow Reported tissue cells Not detected Protein (HPA) HPA →
Cervix Reported tissue cells Not detected Protein (HPA) HPA →
Section 1

What Is the Expected HTR1A Western Blot Band Size?

Use the product-observed 46.1 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
46.1 kDaMatches the authoritative product WB observation.
46.1 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected HTR1A appearancePlan around 46.1 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band46.1 kDa; use this as the primary experimental expectation.
Calculated mass46.1 kDa from UniProt P08908; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with PA1647.
Why is my band missing or off?
SituationLikely causeNext action
46.1 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.
Section 2

Real Curated HTR1A Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateCerebellum
Gel %12-15%
Load20-30 µg total protein per lane
TransferSemi-dry, standard transfer
Membrane0.45 µm PVDF
Blocking5% non-fat milk or 5% BSA in TBST
PrimaryPA1647 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 4

Advanced HTR1A Western Blot Tips

Deeper troubleshooting and optimisation questions for HTR1A, answered from its protein features.

Which band should guide the blot?
Use 46.1 kDa, the observation attached to the authoritative PA1647 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 46.1 kDa expectation.
Which positive control should I start with?
Start with Cerebellum, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Bone marrow 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 HTR1A Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should PA1647 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: PMC12155171, PMC10547165, PMC11153829.
Boster reagents

HTR1A Western Blot Reagents

Human/Rat-reactive HTR1A Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for HTR1A using PA1647; observed band 46.1 kDa
Anti-5HT1A Receptor/HTR1A Antibody Picoband®
Cat # PA1647
Reactivity: Human, Rat

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.