KIF1C rabbit pAb
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],
Product Specifications
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]
UniProt
O43896
Swiss Prot
O43896
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human protein . at AA range: 1110-1190
Target
KIF1C
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
121kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
121kD
Fragment
IgG
Subcellular Location
Cytoplasm, cytoskeleton .
Gene ID (Human)
10749
Available Sizes
Curated Selection
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