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- Table of Contents
KIF7 · Western blot design guide
KIF7 Western Blot Planning Guide
Plan a KIF7 Western blot around the catalog-observed 150.6 kDa band, image-backed A04321-3 evidence, HPA controls, and verified protocol records.
Evidence assembled July 2026 · For research use; verify linked source records and product datasheet before use
KIF7 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 | 150.6 kDa | |
| Observed band | Not reported — verify product WB image | |
| Gel | 8-10% | |
| Positive control | Skin | |
| Negative control | Bone marrow |
Important caveats
Reasons your observed band may differ from the expected size.
| ⓘ | Calculated mass | 150.6 kDa |
| ⓘ | Localization | Cell projection, cilium / Cytoplasm, cytoskeleton, cilium basal body |
| ⓘ | Processing / PTM | Record-dependent |
| ⓘ | Reactivity | Human |
Section 1
Real Curated KIF7 Western Blot Protocols
Start with the molecular-weight rule, then compare verified publication-derived conditions.
| Sample / lysate | Pancreas |
| Gel % | 8-10% |
| Load | 20-30 µg total protein per lane |
| Transfer | Wet/tank, extended transfer |
| Membrane | 0.45 µm PVDF |
| Blocking | 5% non-fat milk or 5% BSA in TBST |
| Primary | A04321-3 at datasheet starting dilution |
| Primary incubation | Overnight at 4 °C with gentle agitation |
| Secondary | Species-matched HRP conjugate at validated dilution |
| Wash | 3 × 5 min in TBST |
| Detection | Chemiluminescent substrate |
| Exposure | Bracket exposures to avoid saturation |
Section 2
What Is the Expected KIF7 Western Blot Band Size?
Use the product-observed 150.6 kDa band as the primary planning value and retain the UniProt calculated mass as context.
| 150.6 kDa | Matches the authoritative product WB observation. |
| 150.6 kDa calculated | Use as UniProt context, not as a replacement observed band. |
| Unexpected additional signal | Do not assign identity without orthogonal positive/negative controls. |
💡Expected KIF7 appearancePlan around 150.6 kDa and keep the calculated mass as supporting context.
| Catalog-observed band | 150.6 kDa; use this as the primary experimental expectation. |
| Calculated mass | 150.6 kDa from UniProt Q2M1P5; retain as context. |
| Gel selection | 8-10%; shared with the recommended protocol and poster. |
| Specificity check | Compare the lead HPA positive and negative controls with A04321-3. |
| Situation | Likely cause | Next action |
|---|---|---|
| 150.6 kDa | Matches the authoritative product WB observation. | Confirm with orthogonal controls and the linked product record. |
| Additional band | May reflect processing, modification, or non-specific signal. | Run a dilution series and compare positive/negative controls. |
| Weak signal | Target abundance or transfer may be limiting. | Verify transfer, increase positive-control abundance, and bracket exposure. |
Experiment evidence
Western blot images showing KIF7 band
A04321-3 · KIF7
← swipe / scroll for more images →
Real WB data behind the band-size expectations in this section.
Sample controls for KIF7 Western blot
🧪Use Skin as the first positive-control candidate and Bone marrow as the HPA Not detected negative candidate.
Positive control: Skin (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 KIF7
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
| Tissue | Cell type | Level | Evidence | Source |
|---|---|---|---|---|
| Skin | Reported tissue cells | High | Protein (HPA) | HPA → |
| Stomach | Reported tissue cells | High | Protein (HPA) | HPA → |
| Pancreas | Reported tissue cells | High | Protein (HPA) | HPA → |
| Placenta | Reported tissue cells | High | Protein (HPA) | HPA → |
Section 3
Advanced KIF7 Western Blot Tips
Deeper troubleshooting and optimisation questions for KIF7, answered from its protein features.
Which band should guide the blot?
Use 150.6 kDa, the observation attached to the authoritative A04321-3 WB record.
How should calculated mass be interpreted?
Treat the UniProt calculated mass as context; it does not replace the catalog-observed 150.6 kDa expectation.
Which positive control should I start with?
Start with Skin, 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 8-10% consistently across the quick facts, protocol table, and poster.
What transfer method to use for KIF7 Western blot?
Use the transfer method in the recommended protocol and verify transfer before blocking.
How should A04321-3 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
KIF7 Western Blot Reagents
Human-reactive KIF7 Western blot reagents with authoritative product imagery.
Real WB data
Anti-KIF7 Antibody Picoband®
Cat # A04321-3
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
- UniProt Q2M1P5
- Human Protein Atlas — KIF7
- A04321-3 product record
- PMC7606012 — Human papillomavirus 16 (HPV 16) E6 but not E7 inhibits the antitumor activity of LKB1 in lung cancer cells by downregulating the expression of KIF7 (Thoracic cancer, 2020)
- PMC4829432 — T-box3 is a ciliary protein and regulates stability of the Gli3 transcription factor to control digit number (eLife, 2016)
- PMC4180749 — Downregulation of the gli transcription factors regulator Kif7 facilitates cell survival and migration of choriocarcinoma cells (PloS one, 2014)