Epilepsy, Progressive Myoclonus Type 2A (Lafora Disease, EPM2A, Laforin, LD, LDE, EPM2, MELF, LAFPTPase, FLJ11207, KIAA0766)

• Catalog number
  GEN608822
• Price
  Please ask
• Size
  100ug

• Also known as
  Epilepsy, Progressive Myoclonus Type 2A
• Other names
  Epilepsy, progressive myoclonus type 2A, Lafora disease (laforin); Laforin; laforin; LAFPTPase; lafora PTPase; OTTHUMP00000017360; OTTHUMP00000017361; epilepsy, progressive myoclonus type 2, Lafora disease (laforin); epilepsy, progressive myoclonus type 2A, Lafora disease (laforin); Lafora PTPase
• Category
  Antibodies
• Subcategory
  Mnoclonal antibodies
• Gene name
  EPM2A; EPM2A; EPM2; MELF; N/A
• Gene name synonims
  EPM2A; EPM2A; EPM2; MELF; N/A
• Other gene names
  EPM2A; EPM2A; EPM2; MELF; N/A
• Clonality
  Monoclonal
• Immunoglobulin isotype
  IgG2b
• Clone
  9H116
• Host organism
  Mouse (Mus musculus)
• Source organism
  Human (Homo sapiens)
• Species reactivity
  Human (Homo sapiens); Due to limited knowledge and inability for testing each and every species, the reactivity of the antibody may extend to other species which are not listed hereby.
• Specificity and cross reactivity
  Detects endogenous human Laforin at 38kD using Western blot. ; Since it is not possible to test each and every species our knowledge on the corss reactivity of the antibodies is limited. This particular antibody might cross react with speacies outside of the listed ones.
• Purification method
  Affinity Purified by Protein G immunoaffinity chromatography.
• Form Appearance
  Supplied as lyophilized from a 0.2um sterile-filtered solution in PBS with 5% trehalose. Reconstitute in PBS containing 0.02% sodium azide.
• Concentration
  N/A
• Storage and shipping
  Lyophilized powder may be stored the antibody should be stored at -20 degrees Celsius.. Stable for 12 months the antibody should be stored at -20 degrees Celsius.. Reconstitute by adding sterile 40-50% glycerol, aliquot and For optimal long term storage, the antibody should be kept at -20 degrees Celsius. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
• Tested applications
  Western Blot (WB)

• Gene target
  Epilepsy   Progressive   Myoclonus   Lafora   Disease   EPM2A   Laforin   LDE   EPM2   MELF   LAFPTPase   FLJ11207   KIAA0766  
• Gene symbol
  EPM2AIP1, EPM2A, EPM2A-DT
• Short name
  Epilepsy, Progressive Myoclonus 2A (Lafora Disease, EPM2A, Laforin, LD, LDE, EPM2, MELF, LAFPTPase, FLJ11207, KIAA0766)
• Alternative name
  Anti-Epilepsy, Progressive Myoclonus Type 2A (Lafora Disease, EPM2A, Laforin, LD, LDE, EPM2, MELF, LAFPTPase, FLJ11207, KIAA0766)

Gene info

• Identity
  HGNC:19735
• Gene
  EPM2AIP1
• Long gene name
  EPM2A interacting protein 1
• Synonyms gene name
  • EPM2A (laforin) interacting protein 1
• Synonyms
  • KIAA0766
  • FLJ11207
• Synonyms name
  • laforin interacting protein 1
• GenBank acession
  • AB018309
• Locus
  3p22.2
• Discovery year
  2003-03-26
• Entrez gene record
  9852
• RefSeq identity
  • NM_014805
• VEGA ID
  OTTHUMG00000185486

Gene info

• 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

Gene info

• Identity
  HGNC:48990
• Gene
  EPM2A-DT
• Long gene name
  EPM2A divergent transcript
• Synonyms gene
  • FBXO30-DT
• Synonyms gene name
  • FBXO30 divergent transcript
• Locus
  6q24.3
• Discovery year
  2020-01-17
• Entrez gene record
  100507557
• Pubmed identfication
  • 32079618
• RefSeq identity
  • NR_038244
• Classification
  • Divergent transcripts

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