Polyclonal Antibodies
Anti-EPM2A Rabbit Polyclonal Antibody for WB, ELISA - O95278
Item Number : CM0028396
Price varies based on specs and customizations
- Application
- WB, ELISA
- Cross Reactivity
- Human, Mouse, Rat
- Protein Weight
- 37kDa
Shipping:
Contact us to get shipping details Enjoy On-time Dispatch Guarantee.
Why Choose Us
Easy ordering process, quality products, and dedicated support for your business success.
Core Product Specifications and Parameters
| Parameter | Value |
|---|---|
| Product Name | EPM2A Rabbit pAb |
| Remarks/Alias | EPM2; MELF; EPM2A |
| Species | Human |
| Gene ID (Human) | 7957 |
| Gene ID | 7957 |
| Immunogen | Recombinant fusion protein containing a sequence corresponding to amino acids 244-331 of human EPM2A (NP_005661.1) |
| Source | Rabbit |
| Category | Polyclonal Antibodies |
| Application | WB, ELISA |
| Cross Reactivity | Human, Mouse, Rat |
| SWISS | O95278 |
| Protein Weight | 37kDa |
| Shipping | Ice bag |
Biological Background: Laforin Function and Localization
- Laforin is a dual-specificity phosphatase encoded by the EPM2A gene, also known as glucan phosphatase or glycogen phosphatase. It plays a critical role in glycogen metabolism by dephosphorylating glycogen, thus preventing hyperphosphorylation and the formation of insoluble aggregates, which are hallmarks of Lafora disease. Related references: PMID:16901901, PMID:23922729, PMID:25538239
- Laforin exhibits strong phosphatase activity towards complex carbohydrates in vitro and can also dephosphorylate phosphotyrosine and synthetic substrates like pNPP, but shows low activity towards phosphoserine/phosphothreonine. Related references: PMID:11001928, PMID:11220751, PMID:11739371
- It forms a complex with NHLRC1/malin and HSP70, which targets misfolded proteins for degradation via the ubiquitin-proteasome system, and also serves as a scaffold to promote PPP1R3C/PTG ubiquitination. Related references: PMID:23922729
- Additionally, laforin promotes proteasome-independent protein degradation through the macroautophagy pathway. Related references: PMID:20453062
- The protein exists in multiple isoforms; isoform 2 lacks phosphatase activity and may act as a dominant-negative regulator of isoform 1 and isoform 7. Related references: PMID:18617530, PMID:22036712
- Laforin is widely expressed in heart, skeletal muscle, kidney, pancreas, and brain, with isoform 4 also expressed in placenta.
- Subcellularly, laforin localizes to the cytoplasm, endoplasmic reticulum membrane, cell membrane, and nucleus.
- Mutations in EPM2A cause Lafora disease, a progressive myoclonus epilepsy with glycogen inclusion bodies (Lafora bodies).
Experimental Guidance and Technical Tips
- The immunogen spans amino acids 244–331, a region present in full-length laforin. This polyclonal antibody is likely to detect multiple isoforms that include this epitope.
- For Western blot, the expected molecular weight is approximately 37 kDa. Validate band specificity using positive controls such as human brain or skeletal muscle lysates, and consider pre-adsorption or peptide blocking to confirm signal.
- For ELISA, the recombinant immunogen can serve as a capture antigen or positive control. Ensure proper coating and detection conditions are optimized.
- Cross-reactivity with mouse and rat has been reported, but users should verify performance in their specific sample type and application.
CamelBio: Your One-Stop Sourcing Bridge
CamelBio supports diagnostic manufacturers and research laboratories with a comprehensive portfolio of IVD raw materials, including validated antibody pairs, optimized monoclonal and polyclonal antibodies, and bulk ancillary reagents. For targets such as EPM2A/laforin implicated in neurological and metabolic disorders, we specialize in sourcing rare-target raw materials to accelerate your assay development. Our integrated services help streamline your workflow from concept to clinic.
Product Datasheet
Anti-EPM2A Rabbit Polyclonal Antibody for WB, ELISA - O95278
REQUEST A QUOTE
Our professional team will reply to you within one business day. Please feel free to contact us!