HSPD1 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 61.1 kDa observed
Observed band 61.1 kDa observed
Gel 12-15%
Positive control ⓘ Adrenal gland
Negative control ⓘ Seminal vesicle
Important caveats
Reasons your observed band may differ from the expected size.
ⓘCalculated mass61.1 kDa
ⓘLocalizationMitochondrion matrix
ⓘProcessing / PTMRecord-dependent
ⓘReactivityHuman / Mouse / Rat
Section 1

Real Curated HSPD1 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateAdrenal gland
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
PrimaryM01280-3 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 HSPD1 Western Blot Band Size?

Use the product-observed 61.1 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
61.1 kDaMatches the authoritative product WB observation.
61.1 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected HSPD1 appearancePlan around 61.1 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band61.1 kDa; use this as the primary experimental expectation.
Calculated mass61.1 kDa from UniProt P10809; retain as context.
Gel selection12-15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with M01280-3.
Why is my band missing or off?
SituationLikely causeNext action
61.1 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 HSPD1 Western blot

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

HPA tissue expression evidence for HSPD1

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
Adrenal gland Reported tissue cells High Protein (HPA) HPA →
Colon Reported tissue cells High Protein (HPA) HPA →
Appendix Reported tissue cells High Protein (HPA) HPA →
Bronchus Reported tissue cells High Protein (HPA) HPA →

Undetected expression · recommended negative controls

Tissue Cell type Level Evidence Source
Seminal vesicle Reported tissue cells Not detected Protein (HPA) HPA →
Skeletal muscle Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced HSPD1 Western Blot Tips

Deeper troubleshooting and optimisation questions for HSPD1, answered from its protein features.

Which band should guide the blot?
Use 61.1 kDa, the observation attached to the authoritative M01280-3 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 61.1 kDa expectation.
Which positive control should I start with?
Start with Adrenal gland, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Seminal vesicle 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 HSPD1 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should M01280-3 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

HSPD1 Western Blot Reagents

Human/Mouse/Rat-reactive HSPD1 Western blot reagents with authoritative product imagery.

Real WB dataWestern blot validation image for HSPD1 using M01280-3; observed band 61.1 kDa
Anti-Hsp60/HSPD1 Antibody Picoband® (monoclonal, 6G2)
Cat # M01280-3
Real WB dataWestern blot validation image for HSPD1 using PA1106; observed band 61.1 kDa
Anti-HSP60/HSPD1 Antibody Picoband®
Cat # PA1106
Real WB dataWestern blot validation image for HSPD1 using PB9337; observed band 61.1 kDa
Anti-Hsp60/HSPD1 Antibody Picoband®
Cat # PB9337

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.