KIF1C rabbit pAb

• Background :

  Kinesin family member 1C (KIF1C) Homo sapiens The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. Mutations in this gene are a cause of spastic ataxia 2, autosomal recessive. [provided by RefSeq, May 2014]

• Description :

  Kinesin family member 1C (KIF1C) Homo sapiens The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. Mutations in this gene are a cause of spastic ataxia 2, autosomal recessive. [provided by RefSeq, May 2014],

• UniProt :

  O43896

• Swiss Prot :

  O43896

• Reactivity :

  Human; Mouse; Rat

• Immunogen :

  Synthesized peptide derived from human protein . at AA range: 1110-1190

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Concentration :

  1 mg/ml

• Dilution :

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

• Molecular Weight :

  121kD

• Storage Conditions :

  -20°C/1 year

• Observed Molecular Weight :

  121kD

• Fragment :

  IgG

• Subcellular Location :

  Cytoplasm, cytoskeleton .

• Gene ID (Human) :

  10749