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