MYO1A rabbit pAb

• Background :

  This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1) . Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene. [provided by RefSeq, Dec 2011]

• Description :

  This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene. [provided by RefSeq, Dec 2011],

• UniProt :

  Q9UBC5

• Swiss Prot :

  Q9UBC5

• Reactivity :

  Human; Rat; Mouse

• Immunogen :

  Synthesized peptide derived from human protein . at AA range: 370-450

• Target :

  MYO1A

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

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

• Buffer :

  -20°C/1 year

• Molecular Weight :

  114kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  114kD

• Fragment :

  IgG

• Subcellular Location :

  Cytoplasm, microvillus, brush border, basal plasma membrane, basolateral plasma membrane, apical plasma membrane, lateral plasma membrane, myosin complex, cortical actin cytoskeleton, filamentous actin, plasma membrane raft

• Gene ID (Human) :

  4640