CLDN11 / Claudin-11 · Western blot design guide

Design a Western Blot for CLDN11

Source-linked CLDN11 Western blot protocol options, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-CLDN11 WB antibodies. Everything you need to plan the experiment before you commit precious samples.

Evidence assembled September 2026 · For research use; verify linked source records and product datasheet before use
Western blot protocol sheet for CLDN11: expected band ~22 kDa, hero antibody A08381-1, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable CLDN11 Western blot protocol sheet — expected band ~22 kDa, antibody A08381-1, controls and PMC citations. Open the full CLDN11 WB guide →

CLDN11 Western Blot Experimental Design Guide

Expected bands, source-linked protocol options, controls and antibodies — the at-a-glance facts below, then the full design guide.

Must know before running
Expected band ~22 kDa
Observed band ~22 kDa
Gel 5–20% (catalog A08381-1)
Positive control ⓘ Duodenum (IHC candidate; verify WB) +4 more
Negative control ⓘ Adipose tissue (IHC candidate; verify WB)
Important caveats
Reasons your observed band may differ from the expected size.
PTM Phosphorylated
Caveat Phosphorylation-state controls
Gene-set association MSigDB Hallmark membership
Isoform 1 isoform(s)
Section 1

Source-Linked CLDN11 Western Blot Protocol Options

The A08381-1 protocol combines labelled catalog values with standard starting conditions. Published comparisons retain their own sample, reagent and detection scope.

Recommended Western blot protocol parameters
Sample / lysatehuman HUVEC (catalog A08381-1)
Gel %5–20% (catalog A08381-1)
Load30 ug; reducing conditions (catalog A08381-1)
Transfera nitrocellulose membrane at 150 mA for 50-90 minutes (catalog A08381-1)
Membranenitrocellulose membrane (catalog A08381-1)
Blocking5% non-fat milk/TBS for 1.5 hour at RT (catalog A08381-1)
Primary antibodyA08381-1 · 0.5 μg/mL (catalog A08381-1)
Primary incubationovernight at 4°C (catalog A08381-1)
Secondary antibodygoat anti-rabbit IgG-HRP, 1:5000 (catalog A08381-1)
Secondary incubation1.5 hour at RT (catalog A08381-1)
WashTBS-0.1%Tween 3 times with 5 minutes each (catalog A08381-1)
DetectionECL (catalog A08381-1)
Section 2

What Is the Expected CLDN11 Western Blot Band Size?

CLDN11 is predicted at 22 kDa, and antibody QC reports a ~22 kDa band; its documented features do not establish another migration pattern.

What am I looking at on my blot?
Band at ~22 kDaMatches the reported CLDN11 band and UniProt predicted mass
Faint ~22 kDa band in soluble extractCLDN11 is a multi-pass membrane protein that may remain poorly extracted
Stronger ~22 kDa band in membrane-enriched extractConsistent with CLDN11 cell-membrane localization
Near-22 kDa doubletCould reflect phosphorylation at Ser197 or Ser198; band identity needs confirmation
💡Expected CLDN11 appearanceUniProt predicts 22 kDa, and antibody QC reports a ~22 kDa band; confirm identity with an appropriate positive control or CLDN11 depletion.
How each factor affects band size
UniProt predicted massPlaces full-length CLDN11 near 22 kDa, matching the reported band
Phosphoserine at Ser197May affect migration, but no visible shift is established
Phosphoserine at Ser198May affect migration, but no visible shift is established
Multi-pass membrane localizationCan affect protein recovery; a size shift is not established
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateMembrane-associated CLDN11 may be poorly extractedCheck the membrane fraction and extraction conditions
Band higher than expectedIncomplete solubilization of this multi-pass membrane protein is possibleOptimize denaturation and confirm the band by CLDN11 depletion
Broad smear instead of sharp bandIncomplete membrane-protein solubilization is possibleOptimize detergent extraction and sample preparation
Multiple bandsPhosphorylation at Ser197 or Ser198 is possible, but distinct bands are unprovenCompare phosphatase-treated samples and confirm identity by CLDN11 depletion
Weak or no signalCLDN11 may be poorly recovered from the membrane fractionCheck membrane enrichment and include a CLDN11-positive control

Sample controls for CLDN11 Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for CLDN11 in Western blot, you can use duodenum tissue.
Positive control: Duodenum (IHC candidate; verify WB)
Negative control: Adipose tissue (IHC candidate; verify WB)
Loading controls: Run GAPDH, β-actin, and a total-protein stain alongside the samples.
⚠️Feasibility: As a multi-pass membrane protein, CLDN11 may be easier to detect in membrane-enriched lysate.

HPA tissue expression evidence for CLDN11

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.

Higher expression tissues · candidate positive controls from IHC

TissueCell typeLevelEvidenceSource
Duodenum paneth cells High Protein (IHC) HPA →
Skin fibrohistiocytic cells High Protein (IHC) HPA →
Small intestine paneth cells High Protein (IHC) HPA →
Testis sertoli cells High Protein (IHC) HPA →
Caudate glial cells Medium Protein (IHC) HPA →

Lower expression tissues · IHC evidence, not confirmed WB-negative controls

TissueCell typeLevelEvidenceSource
Adipose tissue adipocytes Not detected Protein (IHC) HPA →
Adrenal gland glandular cells Not detected Protein (IHC) HPA →
Appendix endocrine cells Not detected Protein (IHC) HPA →
Bone marrow hematopoietic cells Not detected Protein (IHC) HPA →
Breast adipocytes Not detected Protein (IHC) HPA →
Section 3

Advanced CLDN11 Western Blot Tips

Deeper troubleshooting and optimisation questions for CLDN11, answered from its protein features.

How should CLDN11 band migration be interpreted?
Band shift · Use the separately labelled calculated mass and catalog-observed evidence above. A sequence annotation does not establish an observed migration shift. Verify target identity with orthogonal controls.
Could a second CLDN11 band be a listed isoform?
Isoforms · The supplied UniProt record lists one isoform and no alternative sequence. It therefore provides no basis to assign another band to a documented CLDN11 isoform.
Which CLDN11 phosphorylation sites matter when interpreting a band shift?
PTM · UniProt lists phosphoserines at positions 197 and 198 in the 207-residue sequence. These are UniProt coordinates; paper or antibody numbering may differ. Their annotation alone cannot explain an observed mass difference.
Does this guide establish induction of CLDN11?
Induction · No general induction response is established by this guide. A pathway or gene-set association is not evidence of induction in a particular specimen. Verify the relevant treatment and control in a target-specific experiment.
What transfer method to use for CLDN11 Western blot?
Transfer · CLDN11 is a ~22 kDa multi-pass membrane protein. Choose transfer conditions that retain proteins near 22 kDa, and verify transfer at that size. The supplied features do not establish one optimal transfer method.
How should blocking be optimized?
Blocking · Standard workflow guidance: follow the A08381-1 datasheet where specified. Otherwise compare 5% milk or 5% BSA in TBST; for a phospho-specific assay start with BSA. Optimize background and specific signal with matched controls.
How should CLDN11 be quantified?
Quantitation · Standard workflow guidance: quantify only a validated target band within the linear exposure range. Use consistent sample preparation and loading, retain biological replicates, and avoid interpreting saturation or loading differences as regulation.
Should CLDN11 appear above its predicted 22 kDa mass?
Interpretation · The supplied apparent band is ~22 kDa, matching the predicted mass. Phosphorylation is annotated, but its presence alone does not establish a visible shift.

CLDN11 localizes to the cell membrane and tight junctions. Use the same sample preparation and fraction across samples when comparing its ~22 kDa band; differences in membrane recovery can affect the comparison.

The record lists interactions with OCLN and, by similarity, TSPAN3. Those interactions do not establish that a higher Western-blot band is a CLDN11 oligomer. Confirm the band’s identity before assigning it to an interaction or modification.
Boster reagents

CLDN11 Western Blot Antibodies

Catalog antibodies with Western blot application and product-specific WB images. Evaluate suitability with the reported sample, controls and experimental conditions.

Real WB data Western blot analysis of CLDN11 using anti-CLDN11 antibody (A08381-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HUVEC whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLDN11 antigen affinity purified polyclonal antibody (Catalog # A08381-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CLDN11 at approximately 22 kDa. The expected band size for CLDN11 is at 22 kDa.
Anti-CLDN11 Antibody Picoband®
Cat # A08381-1
Real WB data Western blot analysis of Oligodendrocyte Specific Protein expression in SH-SY5Y cell lysate.
Anti-Claudin 11 CLDN11 Monoclonal Antibody
Cat # M08381

Two the supplier anti-CLDN11 antibodies have WB images. A08381-1 shows an approximately 22 kDa band in human HUVEC lysate at 0.5 μg/mL. M08381 shows a blot using SH-SY5Y lysate, but its supplied caption gives no band size or assay conditions.

Which to pick: Choose A08381-1 for the documented human HUVEC WB example. Consider M08381 if you need catalogued mouse or rat reactivity; its supplied WB example uses SH-SY5Y lysate and does not document mouse or rat samples.

Source: BosterBio CLDN11 gene-info card — filtered to Western-blot-capable antibodies; each card shows that product's actual WB validation figure.