EPM2A Antibody - N-terminal region: FITC (ARP63377_P050-FITC)
Product Specifications
Gene Name
Epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Gene Aliases
EPM2, MELF
Gene ID
7957
Swiss Prot
O95278-2
Host
Rabbit
Reactivity
Human, Mouse, Rat, Cow, Dog, Pig, Rabbit
Immunogen
The immunogen is a synthetic peptide directed towards the N-terminal region of Human EPM2A
Target
This gene encodes a dual-specificity phosphatase that associates with polyribosomes. The encoded protein may be involved in the regulation of glycogen metabolism. Mutations in this gene have been associated with myoclonic epilepsy of Lafora. Alternative splicing results in multiple transcript variants.
Partner Proteins
NHLRC1; EPM2A; PPP1R3D; PRKAA1; STUB1; PRKAB2; PRKAA2; PPP1R3C; UBC; GSK3B; NFU1; EPM2AIP1; UBE2D1; HSPA5
Clonality
Polyclonal
Conjugation
FITC: Fluorescein Isothiocyanate
Type
Polyclonal Antibody
Applications
WB
Purification
Affinity Purified
Concentration
0.5 mg/mL
Homology
Cow: 100%; Dog: 93%; Human: 100%; Mouse: 86%; Pig: 86%; Rabbit: 93%; Rat: 86%
Format
Liquid. Purified antibody supplied in 1x PBS buffer.
Reconstitution
All conjugated antibodies should be stored in light-protected vials or covered with a light protecting material (i.e. aluminum foil) . Conjugated antibodies are stable for at least 12 months at 4C. If longer storage is desired (24 months), conjugates may be diluted with up to 50% glycerol and stored at -20C to -80C. Freezing and thawing conjugated antibodies will compromise enzyme activity as well as antibody binding.
Molecular Weight
34kDa
Shipping Conditions
Wet Ice
Protein Length
317
NCBI Gene Symbol
EPM2A
Protein Name
Laforin
Curated Selection
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items
