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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KIF1C-20-RE | 20 (40 μL) | 200 μL |  |
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| KIF1C-20-OR | 20 (40 μL) | 200 μL |  |
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| KIF1C-20-GO | 20 (40 μL) | 200 μL |  |
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| KIF1C-20-GR | 20 (40 μL) | 200 μL |  |
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| KIF1C-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : KIF1C
Gene Name : Kinesin family member 1C
Chromosome : CHR 17: 499,794,7-502,839,8
Locus : 17p13.2
Alt. Genes : ABI2
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