Anti-Laforin antibody (50-100 aa) (STJ13100168)

SKU:
STJ13100168-100

Shipping:
Free Shipping
Current Stock:
Host: Rabbit
Applications: IHC/WB
Reactivity: Human
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit polyclonal antibody anti-Laforin (50-100 aa) is suitable for use in Immunohistochemistry and Western Blot research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: Lyophilised
Purification: IgG purified
Dilution Range: IHC, WB (confirmed by recombinant protein). A dilution of 1:300 to 1:2000 is recommended. The optimal dilution should be determined by the end user. Not yet tested in other applications.
Storage Instruction: Maintain the lyophilised/reconstituted antibodies frozen at-20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, Glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.
Gene Symbol: EPM2A
Gene ID: 7957
Uniprot ID: EPM2A_HUMAN
Immunogen Region: 50-100 aa
Specificity: Specific for Laforin.
Immunogen: A synthetic peptide from aa region 50-100 of mouse Laforin conjugated to an immunogenic carrier protein was used as the antigen. The antigen is homologous in human.
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

12 months for antibodies. 6 months for ELISA Kits. Please see website T&Cs for further guidance