Anti-EPM2A antibody (243-331aa) [k2A3] (STJA0041486)

SPECIFICATIONS
ClonalityMonoclonal
HostMouse
ConjugationUnconjugated
IsotypeIgG1k
ImmunogenRecombinant human EPM2A (243-331aa) purified from E. coli
STJA0041486
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General Information

Short DescriptionMouse monoclonal anti-EPM2A (243-331aa) for use in ELISA, WB, ICC and IF in Human samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsELISA/WB/ICC/IF
HostMouse
ReactivityHuman
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone IDk2A3
IsotypeIgG1k
ConjugationUnconjugated
Concentration1 mg/mL
PurificationBy protein-G affinity chromatography
FormulationLiquid in phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% Glycerol
Storage InstructionFor short term storage, keep at +2C to +8C for up to 1 week. For long term storage, aliquot and store at-20C, and avoid repeat freeze-thaw cycles.

Target Information

Gene SymbolEPM2A
Gene ID7957
Uniprot IDEPM2A_HUMAN
Accession NumberNP_005661
ImmunogenRecombinant human EPM2A (243-331aa) purified from E. coli
Immunogen Region243-331aa

Additional Info

Tissue Specificity Expressed in heart, skeletal muscle, kidney, pancreas and brain. Isoform 4 is also expressed in the placenta.
Post Translational Modifications Polyubiquitinated by NHLRC1/malin. Phosphorylation on Ser-25 by AMPK affects the phosphatase activity of the enzyme and its ability to homodimerize and interact with NHLRC1, PPP1R3C or PRKAA2.
Function Plays an important role in preventing glycogen hyperphosphorylation and the formation of insoluble aggregates, via its activity as glycogen phosphatase, and by promoting the ubiquitination of proteins involved in glycogen metabolism via its interaction with the E3 ubiquitin ligase NHLRC1/malin. Shows strong phosphatase activity towards complex carbohydrates in vitro, avoiding glycogen hyperphosphorylation which is associated with reduced branching and formation of insoluble aggregates. Dephosphorylates phosphotyrosine and synthetic substrates, such as para-nitrophenylphosphate (pNPP), and has low activity with phosphoserine and phosphothreonine substrates (in vitro). Has been shown to dephosphorylate MAPT. Forms a complex with NHLRC1/malin and HSP70, which suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin-proteasome system (UPS). Acts as a scaffold protein to facilitate PPP1R3C/PTG ubiquitination by NHLRC1/malin. Also promotes proteasome-independent protein degradation through the macroautophagy pathway. Isoform 2: Does not bind to glycogen. Lacks phosphatase activity and might function as a dominant-negative regulator for the phosphatase activity of isoform 1 and isoform 7. Isoform 7: Has phosphatase activity (in vitro).
Protein Name Laforin
Glucan Phosphatase
Glycogen Phosphatase
Lafora Ptpase
Lafptpase
Database Links Reactome: R-HSA-3322077
Reactome: R-HSA-3785653
Cellular Localisation Cytoplasm
Under Glycogenolytic Conditions Localizes To The Nucleus
Isoform 1: Cytoplasm
Endoplasmic Reticulum Membrane
Peripheral Membrane Protein
Cytoplasmic Side
Cell Membrane
Colocalizes With Glycogen Synthase In Punctate Structures In The Cytoplasm
Primarily Associated With Polyribosomes At The Rough Endoplasmic Reticulum
And Also Detected At The Plasma Membrane
Isoform 2: Cytoplasm
Nucleus
Also Found In The Nucleus
Isoform 4: Cytoplasm
Isoform 5: Cytoplasm
Isoform 7: Cytoplasm
Alternative Antibody Names Anti-Laforin antibody
Anti-Glucan Phosphatase antibody
Anti-Glycogen Phosphatase antibody
Anti-Lafora Ptpase antibody
Anti-Lafptpase antibody
Anti-EPM2A antibody

Information sourced from Uniprot.org

Citations

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