
WB analysis of HeLa and 293T lysates (20ug per lane) using EPM2A antibody at a dilution of 1:1,000.
Laforin antibody [k2A3]
GTX53711
Overview
- SupplierGeneTex
- Product NameLaforin antibody [k2A3]
- Delivery Days Customer9
- Application Supplier NoteThe antibody has been tested by ELISA and Western blot analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. Recommended dilution range for Western blot analysis is 1:1,000 ~ 2,000. Recommended starting dilution is 1:1,000.
- ApplicationsWestern Blot, ELISA
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDk2A3
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID7957
- Target nameEPM2A
- Target descriptionEPM2A glucan phosphatase, laforin
- Target synonymsepilepsy, progressive myoclonus type 2, Lafora disease (laforin); epilepsy, progressive myoclonus type 2A, Lafora disease (laforin); EPM2; EPM2A, laforin glucan phosphatase; glucan phosphatase; glycogen phosphatase; lafora PTPase; laforin; LAFPTPase; MELF
- HostMouse
- IsotypeIgG1
- Protein IDO95278
- Protein NameLaforin
- Scientific DescriptionThis gene encodes a dual-specificity phosphatase and may be involved in the regulation of glycogen metabolism. The protein acts on complex carbohydrates to prevent glycogen hyperphosphorylation, thus avoiding the formation of insoluble aggregates. Loss-of-function mutations in this gene have been associated with Lafora disease, a rare, adult-onset recessive neurodegenerative disease, which results in myoclonus epilepsy and usually results in death several years after the onset of symptoms. The disease is characterized by the accumulation of insoluble particles called Lafora bodies, which are derived from glycogen. [provided by RefSeq, Jan 2018]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203