SYCP1 / Synaptonemal complex protein 1 · Western blot design guide

Design a Western Blot for SYCP1

Source-linked SYCP1 Western blot protocol options, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-SYCP1 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 SYCP1: expected band ~114.2 kDa, hero antibody A06079-1, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable SYCP1 Western blot protocol sheet — expected band ~114.2 kDa, antibody A06079-1, controls and PMC citations. Open the full SYCP1 WB guide →

SYCP1 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 ~114.2 kDa
Observed band ~120 kDa
Gel 8% (catalog A06079-1)
Positive control ⓘ Testis (IHC candidate; verify WB)
Negative control ⓘ Adipose tissue (IHC candidate; verify WB)
Important caveats
Reasons your observed band may differ from the expected size.
PTM —
Caveat Testis positive control
Gene-set association MSigDB Hallmark membership
Isoform 1 isoform(s)
Section 1

Source-Linked SYCP1 Western Blot Protocol Options

The A06079-1 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 THP-1, rat testis, rat C6 (catalog A06079-1)
Gel %8% (catalog A06079-1)
Load30 ug; reducing conditions (catalog A06079-1)
Transfera nitrocellulose membrane at 150 mA for 50-90 minutes (catalog A06079-1)
Membranenitrocellulose membrane (catalog A06079-1)
Blocking5% non-fat milk/TBS for 1.5 hour at RT (catalog A06079-1)
Primary antibodyA06079-1 · 0.5 μg/mL (catalog A06079-1)
Primary incubationovernight at 4°C (catalog A06079-1)
Secondary antibodygoat anti-rabbit IgG-HRP, 1:5000 (catalog A06079-1)
Secondary incubation1.5 hour at RT (catalog A06079-1)
WashTBS-0.1%Tween 3 times with 5 minutes each (catalog A06079-1)
DetectionECL (catalog A06079-1)
Section 2

What Is the Expected SYCP1 Western Blot Band Size?

SYCP1 is predicted at 114.2 kDa and observed near 120 kDa; the cause of the difference is not established.

What am I looking at on my blot?
Band near 120 kDaMatches the empirical SYCP1 band; confirm identity with appropriate controls
Band near 114 kDaNear the predicted mass of the 976-residue SYCP1 chain
Band in testis lysateConsistent with SYCP1's role in meiotic chromosome complexes
Weak or absent band in a whole-cell lysateMay reflect limited SYCP1 abundance outside meiotic cells
💡Expected SYCP1 appearanceSYCP1 has a predicted mass of 114.2 kDa and an empirical band near 120 kDa; the cause of the difference is not established, so confirm band identity with appropriate controls.
How each factor affects band size
Predicted molecular massSets the full-chain reference at 114.2 kDa
976-residue sequenceDefines the predicted full-length chain without establishing its apparent migration
Homotetramer assemblyCould contribute to a higher band if assembly survives sample preparation; this is unverified
Coiled-coil structureMight affect apparent migration; no shift is established by the supplied evidence
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateThe sample may contain few cells undergoing meiosisCheck testis lysate as a positive sample and verify protein loading
Band higher than expectedIncomplete disruption of SYCP1 assemblies is possibleReview denaturation conditions and compare with the empirical band near 120 kDa
Band lower than expectedProtein breakdown or nonspecific antibody binding is possibleCheck sample handling and confirm the band with an independent antibody or depletion control
Multiple bandsBreakdown products or nonspecific binding are possibleCompare bands with the 120 kDa reference using an independent antibody or depletion control
Weak or no signalSYCP1 may be scarce outside meiotic chromosome complexesUse a testis positive sample and check extraction, loading, and transfer
Fragments below expected sizeSYCP1 may have degraded during preparationProcess samples promptly with protease inhibitors and confirm fragment identity

Sample controls for SYCP1 Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for SYCP1 in Western blot, you can use testis lysate, where HPA reports medium expression.
Positive control: Testis (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: Because SYCP1 is nuclear and chromosomal, use a lysate that retains nuclear proteins.

HPA tissue expression evidence for SYCP1

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
Testis spermatogonia 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 glandular 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 SYCP1 Western Blot Tips

Deeper troubleshooting and optimisation questions for SYCP1, answered from its protein features.

How should SYCP1 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 SYCP1 band be an annotated isoform?
Isoforms · Only one isoform is supplied, with no alternative sequence listed. A second band cannot be assigned to an annotated SYCP1 isoform from these features alone.
Do annotated modifications explain a SYCP1 band shift?
PTM · No modified residues or glycosylation sites are listed. The supplied features therefore do not identify a modification that explains a shift, but they also do not establish why any particular band migrates differently.
Does this guide establish induction of SYCP1?
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 SYCP1?
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 A06079-1 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 the expected SYCP1 band be quantified?
Quantitation · Quantify the band near the reported 120 kDa position in comparable meiotic samples. Keep sample preparation consistent, since SYCP1 is associated with nuclear chromosomes and synaptonemal complexes.
Why does SYCP1 appear near 120 kDa instead of 114.2 kDa?
Interpretation · The predicted mass is 114.2 kDa, while the reported apparent band is about 120 kDa. The supplied features do not establish the cause of that difference; use the observed position as a guide when identifying the band.

SYCP1 is a meiotic synaptonemal complex component associated with nuclear chromosomes. Choose samples containing meiotic cells and account for its nuclear and chromosomal location when preparing lysates.

SYCP1 is described as a homotetramer with coiled coils, so oligomerization is relevant when assessing a higher band. These features alone do not show that an oligomer persists during Western blotting or identify the band.

The supplied record lists one 976-residue isoform and no propeptide or signal peptide. It does not support assigning a lower band to an annotated isoform or peptide cleavage product. Confirm band identity before interpreting it as SYCP1.
Boster reagents

SYCP1 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 SYCP1 using anti-SYCP1 antibody (A06079-1). 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 THP-1 whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: rat C6 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse TM4 whole cell lysates, Lane 7: mouse RAW264.7 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-SYCP1 antigen affinity purified polyclonal antibody (A06079-1) 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 ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SYCP1 at approximately 120 kDa. The expected band size for SYCP1 is at 114 kDa.
Anti-SYCP1 Antibody Picoband®
Cat # A06079-1

A06079-1 is listed for human, mouse, and rat SYCP1. Its Western blot image shows an approximately 120 kDa band (expected 114 kDa) across the human cell, rat cell and testis, and mouse cell and testis lysates named in the caption. Evidence is limited to this product blot.

Which to pick: A06079-1 is the only listed option and has a Western blot image. Check its reported samples and conditions against your experiment; the pictured lysates do not establish performance in every human, mouse, or rat sample.

Source: BosterBio SYCP1 gene-info card — filtered to Western-blot-capable antibodies; each card shows that product's actual WB validation figure.