Golgi stain
$220/sample (include basic resolution scanning)

Golgi Stain Service: Detailed Visualization of Neurons and Dendritic Architecture
At iHisto, we offer expert Golgi staining to reveal full neuronal morphology — including dendrites, axons, and soma — in rodent brain and spinal cord tissues. This technique remains the gold standard for tracing individual neurons in research involving development, injury, and degeneration.
🧪 Overview
The Golgi stain is a classical silver chromate-based neurohistological method that randomly labels a sparse population of neurons in their entirety. Unlike most stains, it allows visualization of:
Entire neuronal soma, dendritic trees, and axons
Fine branching and spine structures
Neurons isolated from surrounding cellular clutter
At iHisto, our carefully optimized Golgi protocol ensures clear, high-resolution images with strong contrast and minimal background, supporting both academic research and preclinical CNS studies.
⚙️ How the Golgi Stain Works
The stain is based on a silver chromate precipitation reaction between potassium dichromate and silver nitrate. The reaction occurs selectively in a small number of neurons, creating dark black or brown deposits within neuronal structures.
Stain Results:
Neuronal soma, axons, dendrites → black/dark brown
Background → clear or lightly toned
Spines and arborizations → often visible with high clarity
This “sparse labeling” effect enables unobstructed tracing of individual cells.
🧬 Step-by-Step Staining Process
Tissue Preparation
Fresh or formalin-fixed brain or spinal cord is immersed in potassium dichromate for several days.Silver Nitrate Impregnation
Tissue is transferred to silver nitrate solution, forming silver chromate inside neurons.Sectioning
Tissue is sectioned via vibratome (for thick, high-resolution slices) or paraffin microtomy.Mounting and Dehydration
Sections are mounted on slides, then dehydrated and cleared.Coverslipping
Slides are sealed with a silver-compatible medium for long-term storage.
⚠️ Note: Due to biological variability, staining quality may vary; batch QC and careful timing are key.
⚙️ Our Semi-Automated Golgi Workflow
Although Golgi staining is labor-intensive, iHisto standardizes the process with:
Controlled impregnation environment for reproducibility
Batch-specific tracking and QA
Optional vibratome sectioning (80–200 µm) for 3D morphology
Coverslipping optimized for long-term clarity of silver precipitate
🔬 Applications of Golgi Staining
This stain is ideal for full-neuron mapping in CNS research.
Common applications include:
Neurodevelopment – Dendritic growth and arborization
Neurotoxicity – Spine density loss, axonal degeneration
Neurodegeneration – Alzheimer’s, ALS, Parkinson’s models
Comparative neuroanatomy – Brain region analysis
Neuron classification – Based on branching patterns and somatic size
✅ Why Choose iHisto’s Golgi Staining Services
✅ Full structural visualization of neurons and dendrites
✅ Works with both fresh and fixed neural tissue
✅ Vibratome or paraffin sectioning available
✅ Digitization for 3D reconstruction and remote analysis
✅ Technical guidance for brain region targeting or experimental setup
We partner with neuroscience labs, CROs, and pharma teams for precise neuronal imaging.
❓ FAQs
What does the Golgi stain highlight?
Entire neurons — including soma, dendrites, axons, and spines — with high structural fidelity.Can it be used on formalin-fixed tissue?
Yes. While fresh tissue yields optimal results, our protocol adapts for fixed tissue with timing adjustments.What section thickness do you use?
Typically 80–200 µm for vibratome sections, and 5–10 µm for paraffin-based histology.Can slides be scanned?
Yes. We offer high-resolution whole-slide scanning suitable for 3D morphometry or digital archiving.
📩 Request a Quote or Consultation
At iHisto, we deliver precision Golgi staining to support your CNS research goals. From dendritic tracing to axonal injury assessment, our protocol uncovers what standard stains can’t.
👉 Request a Quote or email us at info@ihisto.io