RPS10 / Small ribosomal subunit protein eS10 · Western blot design guide

Design a Western Blot for RPS10

Source-linked RPS10 Western blot protocol options, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-RPS10 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 RPS10: expected band ~18.9 kDa, hero antibody A06898, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable RPS10 Western blot protocol sheet — expected band ~18.9 kDa, antibody A06898, controls and PMC citations. Open the full RPS10 WB guide →

RPS10 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 ~18.9 kDa
Gel 15% (standard starting point)
Positive control ⓘ Breast (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 + Methylated
Caveat Modification-state controls
Gene-set association MSigDB Hallmark membership
Isoform 1 isoform(s)
Section 1

Source-Linked RPS10 Western Blot Protocol Options

The A06898 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 / lysatevarious lysates, (catalog A06898)
Gel %15% (standard starting point)
Load20–30 µg total protein per lane; optimize for abundance (standard starting point)
TransferShort semi-dry transfer; verify retention (standard starting point)
Membrane0.2 µm PVDF (standard starting point)
BlockingBlocking buffer: 3% nonfat dry milk in TBST (catalog A06898)
Primary antibodyA06898 · 1:400 (catalog A06898)
Primary incubationOvernight at 4 °C (standard starting point)
Secondary antibodyGoat Anti-Rabbit IgG, 1:10000 (catalog A06898)
Secondary incubation1 h at room temperature (standard starting point)
Wash3 × 5 min in TBST (standard starting point)
DetectionECL (catalog A06898)
Section 2

What Is the Expected RPS10 Western Blot Band Size?

RPS10 is predicted at 18.9 kDa; its listed modifications could affect mass, but no empirical migration or distinct band pattern is demonstrated.

What am I looking at on my blot?
Single band near 18.9 kDaConsistent with the predicted size of RPS10; confirm identity with antibody controls
Band near 18.9 kDa in cytoplasmic fractionConsistent with cytoplasmic RPS10
Band near 18.9 kDa in nucleolar fractionConsistent with nucleolar RPS10
Weak or absent nucleolar bandCould reflect reduced nucleolar localization, which requires methylation
💡Expected RPS10 appearanceRPS10 has a predicted mass of 18.9 kDa, but no empirical band size is supplied; use band identity controls to assess any signal near that size.
How each factor affects band size
UniProt predicted massPlaces unmodified RPS10 near 18.9 kDa
Phosphotyrosine at residue 12Adds a phosphate; a visible migration change is not established
Phosphoserine at residue 146Adds a phosphate; a visible migration change is not established
Omega-N-methylarginine at residue 153Adds a methyl group; a visible migration change is not established
Symmetric dimethylarginine at residues 158 and 160Adds methyl groups; a visible migration change is not established
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateRPS10 localization across cytoplasm and nucleolus may affect recoveryCheck loading and compare cytoplasmic and nuclear fractions
Band higher than expectedThe listed modifications do not establish a large size shiftVerify antibody specificity and compare with a validated RPS10 control
Band lower than expectedNo signal peptide or propeptide cleavage is listedCheck band identity with an independent RPS10 antibody
Multiple bandsModification sites are listed, but distinct migrating forms are not establishedValidate each band with an independent antibody or RPS10 depletion
Weak or no signalSubcellular distribution may reduce RPS10 abundance in the sampled fractionCheck loading and sample cytoplasmic and nucleolar fractions

Sample controls for RPS10 Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for RPS10 in Western blot, you can use breast tissue, which has high HPA expression.
Positive control: Breast (IHC candidate; verify WB)
Negative control: Adipose tissue (IHC candidate; verify WB)
Loading controls: Run GAPDH, β-actin, and a total-protein stain alongside.
⚠️Feasibility: Whole-cell lysate is suitable for this intracellular protein; HPA reports no detection in adipose tissue.

HPA tissue expression evidence for RPS10

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
Breast glandular cells High Protein (IHC) HPA →
Duodenum glandular cells High Protein (IHC) HPA →
Esophagus squamous epithelial cells High Protein (IHC) HPA →
Pancreas exocrine glandular cells High Protein (IHC) HPA →
Small intestine glandular cells High Protein (IHC) HPA →

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

TissueCell typeLevelEvidenceSource
Adipose tissue adipocytes Not detected Protein (IHC) HPA →
Heart muscle cardiomyocytes Not detected Protein (IHC) HPA →
Ovary follicle cells Not detected Protein (IHC) HPA →
Skeletal muscle myocytes Not detected Protein (IHC) HPA →
Smooth muscle smooth muscle cells Not detected Protein (IHC) HPA →
Section 3

Advanced RPS10 Western Blot Tips

Deeper troubleshooting and optimisation questions for RPS10, answered from its protein features.

Where should the main RPS10 band appear?
Band shift · The calculated mass is 18.9 kDa. No observed band position is supplied, so use 18.9 kDa as a reference, not a confirmed apparent mass.
Could an RPS10 isoform explain a second band?
Isoforms · The supplied entry lists one isoform and no alternative sequence. These features do not support assigning a second band to a listed RPS10 isoform.
Which RPS10 modifications should I consider when interpreting bands?
PTM · UniProt lists phosphotyrosine at position 12, phosphoserine at 146, omega-N-methylarginine at 153, and symmetric dimethylarginine at 158 and 160. These are UniProt sequence coordinates; antibody or paper numbering may differ. Their presence alone does not establish a visible shift.

UniProt lists phosphorylation at Tyr12 and Ser146. Neither site establishes that a shift will be visible, and no observed band position is provided. Treat a shifted band as unresolved without evidence connecting it to RPS10 phosphorylation.
Does this guide establish induction of RPS10?
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.
How should transfer be checked for RPS10?
Transfer · Standard workflow guidance: verify transfer efficiency for the intended target size before interpreting a weak signal. Use total-protein assessment and optimize transfer for the membrane, gel and apparatus; the labelled catalog values take precedence.
How should blocking be optimized?
Blocking · Standard workflow guidance: follow the A06898 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 I quantify RPS10 across cellular fractions?
Quantitation · RPS10 is reported in both cytoplasm and nucleolus. Quantify matched fractions separately and keep sample preparation consistent; a change in one fraction can reflect altered localization rather than a change in total RPS10.
Does methylation affect where RPS10 is found?
Interpretation · The supplied features state that methylation is required for RPS10 localization in the granular component of the nucleolus. RPS10 is also reported in the cytoplasm, so compare the same cellular fraction across samples when assessing abundance.

RPS10 is a component of the small ribosomal subunit, and its methylated form interacts with NPM1. Those associations alone do not identify an unexpected Western blot band; avoid assigning it to an RPS10 complex from size alone.
Boster reagents

RPS10 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 various lysates, using RPS10 antibody at 1:400 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit . Exposure time: 30s.
Anti-40S ribosomal protein S10 RPS10 Antibody
Cat # A06898

A06898 is an anti-RPS10 antibody listed for Human, Mouse, and Rat reactivity. Its WB image uses various lysates at 1:400 and 25 µg per lane. The caption does not identify the lysates, and no publication evidence is supplied.

Which to pick: A06898 is the only listed antibody and has a WB image. Consider its stated reactivity and the reported WB conditions for your experiment; the image caption does not establish which species were tested.

Source: BosterBio RPS10 gene-info card — filtered to Western-blot-capable antibodies; each card shows that product's actual WB validation figure.