SYGP1 rabbit pAb

• Background :

  The protein encoded by this gene is a major component of the postsynaptic density (PSD), a group of proteins found associated with NMDA receptors at synapses. The encoded protein is phosphorylated by calmodulin-dependent protein kinase II and dephosphorylated by NMDA receptor activation. Defects in this gene are a cause of mental retardation autosomal dominant type 5 (MRD5) . [provided by RefSeq, Dec 2009]

• Description :

  The protein encoded by this gene is a major component of the postsynaptic density (PSD), a group of proteins found associated with NMDA receptors at synapses. The encoded protein is phosphorylated by calmodulin-dependent protein kinase II and dephosphorylated by NMDA receptor activation. Defects in this gene are a cause of mental retardation autosomal dominant type 5 (MRD5). [provided by RefSeq, Dec 2009],

• UniProt :

  Q96PV0

• Swiss Prot :

  Q96PV0

• Reactivity :

  Human; Rat; Mouse

• Immunogen :

  Synthesized peptide derived from part region of human protein

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000 ELISA 1:5000-20000

• Molecular Weight :

  147kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  147kD

• Fragment :

  IgG

• Subcellular Location :

  Cytoplasm, cytosol, postsynaptic density, intrinsic component of the cytoplasmic side of the plasma membrane, dendritic shaft

• Gene ID (Human) :

  8831