KIF1C Antilichaam

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.

10749

O43896

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 810-960 of human KIF1C (NP_006603.2) .

Unconjugated

Primary Antibodies

Cell Cycle, Immunology, Innate Immunity, Signal Transduction

Affinity purification

HeLa

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 165kDa

IgG

KIF1C

HepG2

293T

K-562

Mouse brain

Kinesin family member 1C

Homo sapiens

KIF1C, SAX2, LTXS1, SATX2, SPAX2, SPG58

WB, IHC

Liquid