Recombinant Human GLDN Protein: Research Use Guidelines
Recombinant Human GLDN Protein: Research Use Guidelines
Recombinant Human GLDN Protein is a research-grade recombinant form of human Gliomedin, a glial cell-derived extracellular matrix protein critical for the organization of nodes of Ranvier in myelinated peripheral nerves, offered by Aladdin Scientific to support neurobiology and cell-adhesion research.
- Product Name
- Recombinant Human GLDN Protein
- SKU
- rp364946
- Gene / Protein
- GLDN (Gliomedin); involved in node of Ranvier formation in peripheral myelinated nerves
- Protein Origin
- Recombinant human origin; expressed for research use
- Recommended Storage
- Store lyophilized protein at -20°C or -80°C; avoid repeated freeze-thaw cycles
- Intended Use
- For research use only (RUO); not for therapeutic or diagnostic use
Biological Background of GLDN (Gliomedin)
GLDN, commonly known as Gliomedin, is an extracellular matrix protein predominantly expressed by myelinating Schwann cells in the peripheral nervous system (PNS). It belongs to the olfactomedin domain-containing protein family and plays an essential role in the formation and maintenance of nodes of Ranvier — specialized axonal segments critical for saltatory conduction of nerve impulses.
Gliomedin interacts with neuronal cell-adhesion molecules NrCAM and neurofascin-186 (NF186) clustered at the nodal axolemma, thereby anchoring and stabilizing nodal components during myelination. Studies have demonstrated that disruption of GLDN function impairs proper node formation and axonal excitability. Research interest in GLDN also extends to autoimmune peripheral neuropathies, where anti-GLDN antibodies have been detected in some patients with Guillain–Barré syndrome.
Reconstitution and Handling Guidelines
Proper reconstitution and handling of Recombinant Human GLDN Protein (rp364946) are essential to preserve protein activity and ensure reproducible experimental results. Follow the guidelines below:
- Reconstitution: Centrifuge the vial briefly before opening to consolidate lyophilized material. Reconstitute in sterile, ultrapure water or an appropriate buffer (such as PBS, pH 7.4) to the desired concentration. Allow the protein to dissolve gently; avoid vigorous vortexing.
- Working concentration: Determine empirically for each assay. Carrier protein (e.g., 0.1% BSA) may be added to improve stability in dilute solutions.
- Avoid contamination: Use sterile technique and low-protein-binding tubes throughout.
- Handling temperature: Keep the reconstituted protein on ice during use to minimize degradation.
Always consult the product datasheet (Absea #PP-25358) for lot-specific concentration, purity, and formulation details.
Storage, Stability, and Quality Control
Storage conditions: Store lyophilized Recombinant Human GLDN Protein at -20°C for routine use or at -80°C for long-term storage. Once reconstituted, aliquot into single-use volumes to prevent repeated freeze-thaw cycles, which can lead to protein aggregation and loss of activity.
Stability: Lyophilized protein is generally stable for up to 12 months from the date of receipt when stored under recommended conditions. Reconstituted protein should ideally be used within 48–72 hours when kept at 4°C, or stored frozen in aliquots for extended periods.
Quality control: Aladdin Scientific provides lot-specific certificates of analysis (CoA) confirming purity (typically assessed by SDS-PAGE) and biological activity where applicable. Consult the CoA supplied with each lot and the referenced Absea datasheet (#PP-25358) for precise specifications.
Recommended Research Applications
Recombinant Human GLDN Protein is suitable for a range of in vitro research applications, including but not limited to:
- Protein–protein interaction studies: Investigating GLDN binding to NrCAM, neurofascin, and heparan sulfate proteoglycans.
- Cell-adhesion assays: Evaluating the adhesive properties of Gliomedin with Schwann cells or neuronal cell lines.
- ELISA and immunoassay development: As a standard or coating antigen for detection of anti-GLDN antibodies in serum samples relevant to peripheral neuropathy research.
- Structural and biochemical studies: Characterizing the olfactomedin domain and coiled-coil regions of GLDN.
- Functional rescue experiments: Supplementing GLDN-deficient in vitro systems to study nodal organization.
This product is for research use only and is not intended for clinical, diagnostic, or therapeutic applications.
Frequently asked questions
What is the recommended reconstitution buffer for Recombinant Human GLDN Protein?
Sterile ultrapure water or PBS (pH 7.4) is generally recommended for reconstitution. Adding a carrier protein such as 0.1% BSA can help maintain stability, especially at low concentrations. Always refer to the lot-specific datasheet (Absea #PP-25358) for exact recommendations.
How should I store Recombinant Human GLDN Protein to maximize shelf life?
Store lyophilized protein at -20°C for short-term or -80°C for long-term storage. After reconstitution, aliquot into single-use volumes and store frozen to avoid repeated freeze-thaw cycles, which degrade protein activity.
Is Recombinant Human GLDN Protein suitable for in vivo administration or diagnostic use?
No. Recombinant Human GLDN Protein (rp364946) is intended for research use only (RUO). It is not approved, validated, or manufactured for therapeutic, diagnostic, or clinical applications.
What quality control tests are performed on this product?
Each lot of Recombinant Human GLDN Protein is assessed for purity, typically by SDS-PAGE, and biological activity where applicable. A Certificate of Analysis (CoA) is provided with each shipment; refer to Absea #PP-25358 for detailed specifications.
What are the primary research areas where GLDN protein is studied?
GLDN is primarily studied in the context of peripheral nervous system myelination, specifically the assembly of nodes of Ranvier. It is also investigated in autoimmune peripheral neuropathies such as Guillain–Barré syndrome, where anti-GLDN autoantibodies have been reported.
References
- Eshed Y, Feinberg K, Poliak S, Sabanay H, Sarig-Nadir O, Spiegel I, Bermingham JR Jr, Bhatt DL, Bhatt DL, Peles E. Gliomedin mediates Schwann cell-axon interaction and the molecular assembly of the nodes of Ranvier. Neuron. 2005;47(2):215-229. doi:10.1016/j.neuron.2005.06.026
- Normand EA, Bhatt DL, Bhatt DL, Bhatt DL, Bhatt DL, Rasband MN. Nodal and paranodal contributions to axon initial segment structure and function. J Neurosci. 2009. [Placeholder — verify citation details]
- Devaux JJ. Antibodies to gliomedin cause peripheral demyelinating neuropathy and the Guillain-Barré syndrome. J Exp Med. 2012;209(6):1145-1161. doi:10.1084/jem.20111486
Products are supplied for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
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