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Monoclonal Antibodies
Anti-Myelin Oligodendrocyte Glycoprotein Monoclonal Antibody for WB, IF/ICC, IHC-P, ELISA - Q16653
Item Number : CM0012557
Price varies based on specs and customizations
- Application
- WB, IF/ICC, IHC-P, ELISA
- Cross Reactivity
- Human, Mouse, Rat
- Protein Weight
- 28kDa
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Core Product Specifications and Parameters
| Parameter | Value |
|---|---|
| Product Name | Myelin oligodendrocyte glycoprotein Rabbit mAb |
| Remarks/Alias | BTN6; BTNL11; MOGIG2; NRCLP7; Myelin oligodendrocyte glycoprotein |
| Species | Human |
| GeneID (Human) | 4340 |
| GeneID | 4340 |
| Immunogen | Synthetic Peptide |
| Source | Rabbit |
| Category | Monoclonal Antibodies |
| Application | WB, IF/ICC, IHC-P, ELISA |
| Cross Reactivity | Human, Mouse, Rat |
| SWISS | Q16653 |
| Protein Weight | 28kDa |
| Shipping | Ice bag |
Biological Background: Myelin Oligodendrocyte Glycoprotein Function and Localization
- Myelin-oligodendrocyte glycoprotein (MOG) is a minor component of the myelin sheath in the central nervous system (CNS), classified under the immunoglobulin superfamily.
- It mediates homophilic cell-cell adhesion, suggesting roles in myelin sheath compaction and maintenance (By similarity).
- MOG is expressed exclusively in the CNS, localized on the surface of myelin and the cytoplasmic membranes of oligodendrocytes.
- The protein serves as a receptor for rubella virus, facilitating viral entry during infection.
- MOG undergoes alternative splicing, generating multiple isoforms that may modulate its adhesive or receptor functions.
- Key structural features include a signal peptide, an extracellular immunoglobulin domain, and a transmembrane helix, anchoring it to the cell membrane.
- Post-translational modifications include N-linked glycosylation and a conserved disulfide bond, which is typical of immunoglobulin-like domains.
- Mutations or polymorphisms in MOG are associated with demyelinating diseases, highlighting its immunopathogenic role in conditions like multiple sclerosis.
Experimental Guidance and Technical Tips
- The synthetic peptide immunogen likely targets a linear epitope; thus, the antibody may recognize denatured protein in WB applications, but native protein recognition in IF/ICC and IHC-P should also be assessed.
- For WB, consider using whole brain or spinal cord lysates from human, mouse, or rat as positive controls, given the CNS-specific expression. A band around 28 kDa is expected.
- In IF/ICC and IHC-P, signal is anticipated on the plasma membrane of oligodendrocytes and myelin sheaths. Co-staining with oligodendrocyte markers (e.g., Olig2, CNPase) is recommended for validation.
- For ELISA, pairing this capture antibody with a different detection antibody targeting a distinct epitope is advisable for optimal sandwich immunoassay development.
- Always validate antibody reactivity in the relevant species and tissue type before scaling up for diagnostic or research use.
CamelBio: Your One-Stop Sourcing Bridge
CamelBio supports diagnostic manufacturers and research laboratories with a comprehensive portfolio of IVD raw materials, including monoclonal and polyclonal antibodies, validated antibody pairs, and bulk ancillary reagents. For targets like Myelin Oligodendrocyte Glycoprotein, which demand high specificity and cross-species reactivity, CamelBio offers optimized sourcing solutions to streamline assay development and production. Whether you require rare target reagents or large-scale supply for clinical diagnostics, CamelBio bridges the gap from concept to commercialization with reliable, one-stop support.
Product Datasheet
Anti-Myelin Oligodendrocyte Glycoprotein Monoclonal Antibody for WB, IF/ICC, IHC-P, ELISA - Q16653
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