EPM2A, NT (Laforin, Lafora PTPase, LAFPTPase)

Products_type

Antibody
Products_short_name

[EPM2A]
Products_name_syn

[Anti -EPM2A, NT (Laforin, Lafora PTPase, LAFPTPase)]
Other_names

[E3 ubiquitin-protein ligase NHLRC1; E3 ubiquitin-protein ligase NHLRC1; E3 ubiquitin-protein ligase NHLRC1; NHL repeat-containing protein 1; NHL repeat containing 1; Malin; NHL repeat-containing protein 1]
Other_gene_names

[NHLRC1; NHLRC1; EPM2A; EPM2B; MALIN; bA204B7.2; EPM2B]
Clonality

Polyclonal
Reactivity

Human
Specificity

Recognizes human EPM2A.
Purity

Affinity Purified Purified by Protein A affinity chromatography.
Form

Supplied as a liquid in PBS, 0.09% sodium azide.
Storage_stability

May be stored at 4 degree C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Tested_application

ELISA (EL/EIA), Immunohistochemistry (IHC)

Identity

HGNC:3413
Gene

EPM2A
Long gene name

EPM2A glucan phosphatase, laforin
Synonyms gene name
- epilepsy, progressive myoclonus type 2, Lafora disease (laforin)
- epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
- EPM2A, laforin glucan phosphatase
Synonyms
- LDE
- LD
GenBank acession
- AF284580
Locus

6q24.3
Discovery year

1998-10-01
Entrez gene record

7957
Pubmed identfication
- 9222970
- 7485240
Classification
- Atypical dual specificity phosphatases
VEGA ID

OTTHUMG00000015747