CXCL12 · Western blot design guide

CXCL12 Western Blot Planning Guide

Plan a CXCL12 Western blot around the catalog-observed 10.7 kDa band, image-backed A00053-1 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 CXCL12 (CXCL12): expected band 10.7 kDa, antibody A00053-1, and guide-derived SDS-PAGE protocol steps
CXCL12 Western blot protocol sheet — expected band 10.7 kDa, antibody A00053-1, controls and PMC citations. Open the full CXCL12 WB guide →

CXCL12 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 10.7 kDa
Observed band Not reported — verify product WB image
Gel 15%
Positive control ⓘ Testis
Negative control ⓘ Appendix
Important caveats
Reasons your observed band may differ from the expected size.
ⓘ Calculated mass 10.7 kDa
ⓘ Localization Secreted
ⓘ Processing / PTM Record-dependent
ⓘ Reactivity Mouse / Rat
Section 1

Real Curated CXCL12 Western Blot Protocols

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

Recommended Western blot protocol parameters
Sample / lysateTestis
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
PrimaryA00053-1 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 CXCL12 Western Blot Band Size?

Use the product-observed 10.7 kDa band as the primary planning value and retain the UniProt calculated mass as context.

What am I looking at on my blot?
10.7 kDaMatches the authoritative product WB observation.
10.7 kDa calculatedUse as UniProt context, not as a replacement observed band.
Unexpected additional signalDo not assign identity without orthogonal positive/negative controls.
💡Expected CXCL12 appearancePlan around 10.7 kDa and keep the calculated mass as supporting context.
How each factor affects band size
Catalog-observed band10.7 kDa; use this as the primary experimental expectation.
Calculated mass10.7 kDa from UniProt P48061; retain as context.
Gel selection15%; shared with the recommended protocol and poster.
Specificity checkCompare the lead HPA positive and negative controls with A00053-1.
Why is my band missing or off?
SituationLikely causeNext action
10.7 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 CXCL12 Western blot

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

HPA tissue expression evidence for CXCL12

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
Testis Reported tissue cells Medium Protein (HPA) HPA →

Undetected expression · recommended negative controls

TissueCell typeLevelEvidenceSource
Appendix Reported tissue cells Not detected Protein (HPA) HPA →
Bone marrow Reported tissue cells Not detected Protein (HPA) HPA →
Section 3

Advanced CXCL12 Western Blot Tips

Deeper troubleshooting and optimisation questions for CXCL12, answered from its protein features.

Which band should guide the blot?
Use 10.7 kDa, the observation attached to the authoritative A00053-1 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 10.7 kDa expectation.
Which positive control should I start with?
Start with Testis, the lead HPA protein-expression candidate.
Which negative control is defensible?
Use Appendix 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 CXCL12 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A00053-1 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

CXCL12 Western Blot Reagents

Mouse/Rat-reactive CXCL12 Western blot reagents with authoritative product imagery.

Real WB data Western blot validation image for CXCL12 using A00053-1; observed band 10.7 kDa
Anti-CXCL12 Antibody Picoband®
Cat # A00053-1

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.

References

  1. UniProt P48061
  2. Human Protein Atlas — CXCL12
  3. A00053-1 product record
  4. PMC12711006 — Multi-omics analysis reveals diagnostic and therapeutic biomarkers for aging phenotypes in ulcerative colitis (PloS one, 2025)
  5. PMC11719110 — Piperine attenuates cancer-associated pain induced by microglial activation via increasing miR-150-50p (Aging, 2024)
  6. PMC6061162 — CXCL12 gene silencing down-regulates metastatic potential via blockage of MAPK/PI3K/AP-1 signaling pathway in colon cancer (Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2018)