ABHD11 rabbit pAb

• Background :

  This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]

• Description :

  This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11. 23. [provided by RefSeq, Mar 2016],

• UniProt :

  Q8NFV4

• Swiss Prot :

  Q8NFV4

• Reactivity :

  Human; Rat; Mouse

• Immunogen :

  The antiserum was produced against synthesized peptide derived from human ABHD11. AA range:161-210

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

  Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.

• Molecular Weight :

  32kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  32kD

• Fragment :

  IgG

• Subcellular Location :

  Mitochondrion

• Other Product Names :

  ABHD11; WBSCR21; PP1226; Abhydrolase domain-containing protein 11; Williams-Beuren syndrome chromosomal region 21 protein

• Gene ID (Human) :

  83451