SOS1 / Son of sevenless homolog 1 · Western blot design guide

Design a Western Blot for SOS1

Real validated SOS1 Western blot protocols, expected-band and isoform facts, troubleshooting for weak or shifted signal, and recommended anti-SOS1 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 SOS1: expected band ~152.5 kDa, hero antibody A00837-1, catalog values and labelled standard workflow; separate PMC comparisons on the guide
Printable SOS1 Western blot protocol sheet — expected band ~152.5 kDa, antibody A00837-1, controls and PMC citations. Open the full SOS1 WB guide →

SOS1 Western Blot Experimental Design Guide

Expected bands, validated protocols, controls and antibodies — the at-a-glance facts below, then the full design guide.

Must know before running
Expected band ~152.5 kDa
Observed band ~170 kDa
Gel 5–20% (catalog A00837-1)
Positive control ⓘ Cerebral cortex (IHC candidate; verify WB) +4 more
Negative control ⓘ Caudate (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 2 isoform(s)
Section 1

Real Curated SOS1 Western Blot Protocols

The A00837-1 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 K562, human THP-1, human HEL (catalog A00837-1)
Gel %5–20% (catalog A00837-1)
Load30 ug; reducing conditions (catalog A00837-1)
Transfera nitrocellulose membrane at 150 mA for 50-90 minutes (catalog A00837-1)
Membranenitrocellulose membrane (catalog A00837-1)
Blocking5% non-fat milk/TBS for 1.5 hour at RT (catalog A00837-1)
Primary antibodyA00837-1 · 0.5 μg/mL (catalog A00837-1)
Primary incubationovernight at 4°C (catalog A00837-1)
Secondary antibodygoat anti-rabbit IgG-HRP, 1:5000 (catalog A00837-1)
Secondary incubation1.5 hour at RT (catalog A00837-1)
WashTBS-0.1%Tween 3 times with 5 minutes each (catalog A00837-1)
DetectionECL (catalog A00837-1)
Section 2

What Is the Expected SOS1 Western Blot Band Size?

SOS1 is predicted at 152.5 kDa and observed near 170 kDa; the cause of that difference is not established.

What am I looking at on my blot?
Band near 170 kDamatches the reported SOS1 band; confirm identity with controls
Band near 152.5 kDanear the predicted sequence mass; identity requires confirmation
Two bands at different positionscould reflect SOS1 isoforms 1 and 2, but their migration is unestablished
Minor band beside the main bandcould reflect a different phosphorylation state; a visible shift is unproven
💡Expected SOS1 appearanceSOS1 has a predicted mass of 152.5 kDa, while antibody QC reports a band near 170 kDa; the cause of the difference is unestablished, so confirm identity with appropriate controls.
How each factor affects band size
Predicted sequence mass152.5 kDa by sequence, versus the reported band near 170 kDa
Isoform 1annotated splice isoform with no supplied individual mass or migration
Isoform 2annotated splice isoform with no supplied individual mass or migration
Alternative splicing of isoforms 1 and 2may alter size, but distinct bands are not established
Why is my band missing or off?
SituationLikely causeNext action
No band in lysateSOS1 signal is undetectedcheck loading, transfer, and a positive control lysate
Band higher than expectedthe reported SOS1 band is near 170 kDa, above its predicted 152.5 kDacompare with the reported band and confirm identity using an independent antibody
Band lower than expectedband identity or isoform contribution is uncertaincheck the molecular weight marker and confirm with an independent antibody
Multiple bandsisoforms 1 and 2 or different phosphorylation states are possible, but their migration is unestablishedcompare bands across controls and verify SOS1 identity
Weak or no signalSOS1 signal may be below detectioncheck loading and transfer, then test a positive control lysate

Sample controls for SOS1 Western blot

🧪HPA-IHC candidate guidance (verify in WB): For positive controls for SOS1 in Western blot, you can use cerebral cortex lysate, which HPA rates High.
Positive control: Cerebral cortex (IHC candidate; verify WB)
Negative control: Caudate (IHC candidate; verify WB)
Loading controls: Run GAPDH, β-actin, and a total-protein stain alongside the samples.
⚠️Feasibility: HPA lists both High and Not detected tissues, making tissue controls feasible.

HPA tissue expression evidence for SOS1

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
Cerebral cortex neuronal cells High Protein (IHC) HPA →
Hippocampus neuronal cells High Protein (IHC) HPA →
Ovary follicle cells High Protein (IHC) HPA →
Placenta trophoblastic cells High Protein (IHC) HPA →
Testis cells in seminiferous ducts High Protein (IHC) HPA →

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

TissueCell typeLevelEvidenceSource
Caudate glial cells Not detected Protein (IHC) HPA →
Cervix glandular cells Not detected Protein (IHC) HPA →
Oral mucosa squamous epithelial cells Not detected Protein (IHC) HPA →
Prostate glandular cells Not detected Protein (IHC) HPA →
Skeletal muscle myocytes Not detected Protein (IHC) HPA →
Section 3

Advanced SOS1 Western Blot Tips

Deeper troubleshooting and optimisation questions for SOS1, answered from its protein features.

How should SOS1 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 the two SOS1 isoforms produce different bands?
Isoforms · Yes. Isoform 2 lacks canonical residues 1–57 and 372–1333 and replaces residues 359–371. It could therefore migrate differently from full-length isoform 1. Check whether the antibody recognizes a region retained in the isoform you want to detect.
Which phosphorylation sites matter when interpreting SOS1 bands?
PTM · UniProt lists phosphoserines at positions 1078, 1082, 1134, 1161, 1178, 1210, 1229, and 1275; RPS6KA3 is specified for 1134 and 1161. These are UniProt canonical-sequence coordinates and may differ from antibody or paper numbering. Their presence does not establish a visible band shift.

Match the antibody’s stated site to the UniProt canonical sequence. Listed phosphoserines are 1078, 1082, 1134, 1161, 1178, 1210, 1229, and 1275; RPS6KA3 is specified for 1134 and 1161. Isoform 2 lacks residues 372–1333, including these sites.
Does this guide establish induction of SOS1?
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 SOS1 Western blot?
Transfer · SOS1 isoform 1 is predicted at 152.5 kDa. Choose and verify transfer conditions that retain and transfer a protein of this size, using a high-molecular-weight marker to assess transfer at the target position.
How should blocking be optimized?
Blocking · Standard workflow guidance: follow the A00837-1 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 SOS1 bands be quantified?
Quantitation · Quantify a consistently identified SOS1 band within the assay’s linear signal range. Because isoform 2 has a large sequence deletion, establish which isoform the antibody detects before combining signals from different bands.
Why might SOS1 appear near 170 kDa instead of 152.5 kDa?
Interpretation · SOS1 has a predicted mass of 152.5 kDa, while the supplied observed band is approximately 170 kDa. The listed phosphorylation sites alone do not establish why it migrates there. Identify the band with a validated SOS1 antibody and an appropriate control.

Consider isoform 2: it lacks residues 1–57 and 372–1333 of the canonical sequence and replaces residues 359–371. A lower band is not identified by size alone. Confirm that the antibody recognizes a retained region and use a suitable specificity control.
Boster reagents

SOS1 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 SOS1 using anti-SOS1 antibody (A00837-1). 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 K562 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 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-SOS1 antigen affinity purified polyclonal antibody (Catalog # A00837-1) 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 SOS1 at approximately 170 kDa. The expected band size for SOS1 is at 152 kDa.
Anti-SOS1 Antibody Picoband®
Cat # A00837-1
Real WB data Western blot analysis of SOS1 using anti-SOS1 antibody (M00837). 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 HEL whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Neuro-2a 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-SOS1 antigen affinity purified monoclonal antibody (M00837) 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 SOS1 at approximately 170 kDa. The expected band size for SOS1 is at 152 kDa.
Anti-SOS1 Rabbit Monoclonal Antibody
Cat # M00837

The catalog reports two anti-SOS1 antibodies with Western blot images using human cell, rat brain and cell, and mouse brain and cell lysates. Both captions report a band near 170 kDa, above the expected 152 kDa; the supplied evidence does not establish band identity independently.

Which to pick: Both A00837-1 and M00837 list human, mouse and rat reactivity and have WB images. Choose by the closest documented sample: A00837-1 includes K562, THP-1 and NIH/3T3; M00837 includes HepG2, SH-SY5Y and Neuro-2a. Both include HEL, rat brain, C6 and mouse brain.

Source: BosterBio SOS1 gene-info card — filtered to Western-blot-capable antibodies; each card shows that product's actual WB validation figure.