DSC1 / Desmocollin-1 · Western blot design guide

Design a Western Blot for DSC1

Source-linked DSC1 Western blot protocol options, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-DSC1 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 DSC1: expected band ~100 kDa, hero antibody M03478, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable DSC1 Western blot protocol sheet — expected band ~100 kDa, antibody M03478, controls and PMC citations. Open the full DSC1 WB guide →

DSC1 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 ~100 kDa
Observed band ~100 kDa
Gel 8% (catalog M03478)
Positive control ⓘ Hair (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 Glycosylated + Phosphorylated
Caveat Precursor versus mature forms
Gene-set association MSigDB Hallmark membership
Isoform 2 isoform(s)
Section 1

Source-Linked DSC1 Western Blot Protocol Options

The M03478 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 K562, rat lung (catalog M03478)
Gel %8% (catalog M03478)
Load30 ug; reducing conditions (catalog M03478)
Transfera nitrocellulose membrane at 150 mA for 50-90 minutes (catalog M03478)
Membranenitrocellulose membrane (catalog M03478)
Blocking5% non-fat milk/TBS for 1.5 hour at RT (catalog M03478)
Primary antibodyM03478 · 1:500 (catalog M03478)
Primary incubationovernight at 4°C (catalog M03478)
Secondary antibodygoat anti-rabbit IgG-HRP, 1:5000 (catalog M03478)
Secondary incubation1.5 hour at RT (catalog M03478)
WashTBS-0.1%Tween 3 times with 5 minutes each (catalog M03478)
DetectionECL (catalog M03478)
Section 2

What Is the Expected DSC1 Western Blot Band Size?

DSC1 is predicted at 100 kDa and observed at ~100 kDa; its listed processing, glycosylation, and isoforms do not establish additional band positions.

What am I looking at on my blot?
Band at ~100 kDaMatches the observed DSC1 band and the predicted 100 kDa mass; confirm identity with an appropriate control
Band below ~100 kDaCould reflect signal peptide or propeptide cleavage, but its identity requires confirmation
Band above ~100 kDaCould reflect N-linked glycosylation or an uncleaved precursor; neither shift is established here
Multiple bandsCould include isoforms 1A and 1B or differently processed forms; their separation is unestablished
💡Expected DSC1 appearanceDSC1 has a predicted mass of 100 kDa and an empirical band at ~100 kDa; use an appropriate band-identity control when interpreting additional bands.
How each factor affects band size
UniProt predicted massSets a 100 kDa reference, matching the observed ~100 kDa band
N-linked glycosylation at Asn165May affect apparent migration; a visible shift is not established
N-linked glycosylation at Asn546May affect apparent migration; a visible shift is not established
Signal peptide and propeptide cleavageCan make a processed form smaller than its precursor
Splice isoforms 1A and 1BMay differ in size; their masses and band separation are not supplied
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateDSC1 is a cell-membrane desmosomal protein that may be poorly recovered in the lysateCheck membrane-protein extraction and a DSC1-positive sample
Band higher than expectedN-linked glycosylation or incomplete precursor processing is possibleCompare with an N-glycosidase-treated sample and verify band identity
Band lower than expectedSignal peptide or propeptide cleavage is possibleCompare with a DSC1-positive control and check the antibody epitope
Multiple bandsIsoforms 1A and 1B or different processing states are possibleUse an independent DSC1 antibody or depletion control to identify the bands
Weak or no signalLow recovery of membrane-associated DSC1 is possibleCheck extraction, loading, and antibody detection with a positive control
Broad smear instead of sharp bandVariable N-linked glycosylation is possible but unconfirmedCompare treated and untreated samples and confirm DSC1 specificity

Sample controls for DSC1 Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for DSC1 in Western blot, you can use hair tissue, which HPA rates as highly positive.
Positive control: Hair (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 desmosomal membrane protein, DSC1 may require careful extraction for a strong signal.

HPA tissue expression evidence for DSC1

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
Hair cells in internal root sheath High Protein (IHC) HPA →
Ovary follicle cells High Protein (IHC) HPA →
Skin cells in corneal layer High Protein (IHC) HPA →
Cerebellum Bergmann glia - cytoplasm/membrane Medium Protein (IHC) HPA →
Heart muscle cardiomyocytes 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 glandular cells Not detected Protein (IHC) HPA →
Bone marrow hematopoietic cells Not detected Protein (IHC) HPA →
Bronchus respiratory epithelial cells Not detected Protein (IHC) HPA →
Section 3

Advanced DSC1 Western Blot Tips

Deeper troubleshooting and optimisation questions for DSC1, answered from its protein features.

How should DSC1 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.
Can DSC1 isoforms produce different bands?
Isoforms · Possibly. Isoform 1B replaces residues 830..840 and lacks residues 841..894 relative to 1A. This sequence difference could affect band position, but the features do not establish that two bands will resolve on a blot.

Check its epitope against both sequences. An antibody targeting residues 841..894 of isoform 1A would miss isoform 1B, which lacks that region. An epitope within the changed 830..840 segment may also behave differently.
What does DSC1 phosphorylation imply for blot interpretation?
PTM · UniProt lists phosphothreonine at position 385 in the precursor sequence. A phospho-specific antibody must recognize that site; a total DSC1 antibody does not establish its phosphorylation state. Feature presence alone does not demonstrate a visible band shift. Paper or antibody residue numbering may differ from UniProt precursor numbering.
Does this guide establish induction of DSC1?
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 DSC1 Western blot?
Transfer · DSC1 is an approximately 100 kDa, single-pass membrane protein. Use a transfer setup validated for proteins around 100 kDa, then check transfer efficiency on the membrane and residual protein in the gel. The supplied features do not distinguish wet from semi-dry transfer.
How should blocking be optimized?
Blocking · Standard workflow guidance: follow the M03478 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 DSC1 be quantified across samples?
Quantitation · DSC1 localizes to the cell membrane and desmosomes. Keep extraction and fractionation consistent across samples, compare bands within the linear detection range, and normalize to an appropriate loading measure. If the antibody detects both isoforms, define whether the measurement includes one or both.
Does a 100 kDa DSC1 band match its predicted mass?
Interpretation · Yes. The observed band is approximately 100 kDa, matching the supplied prediction. DSC1 also has a signal peptide (1..29), propeptide (30..134), and N-linked glycosylation sites at Asn165 and Asn546. These features alone do not establish a visible shift or explain a mass difference.

Consider the shorter 1B isoform, processing of the signal peptide and propeptide, and glycosylation at Asn165 and Asn546. Check whether the antibody epitope is retained in each candidate form. These features suggest possibilities; they do not identify an unexpected band without further evidence.
Boster reagents

DSC1 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 DSC1 using anti-DSC1 antibody (M03478). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: rat lung tissue 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-DSC1 antigen affinity purified monoclonal antibody (M03478) at 1:500 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 ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DSC1 at approximately 100 kDa. The expected band size for DSC1 is at 100 kDa.
Anti-Desmocollin 1 Rabbit Monoclonal Antibody
Cat # M03478

M03478 is a rabbit monoclonal anti-DSC1 antibody listed for human, mouse, and rat. Its Western blot image shows an approximately 100 kDa band in human K562 cell and rat lung lysates. No publication evidence or mouse blot is supplied.

Which to pick: M03478 is the only listed option. Its supplied Western blot image uses human K562 and rat lung lysates at 1:500 under reducing conditions; mouse reactivity is listed but has no shown blot.

Source: BosterBio DSC1 gene-info card — filtered to Western-blot-capable antibodies; each card shows that product's actual WB validation figure.