The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KLC2-20-RE | 20 (40 μL) | 200 μL |  |
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| KLC2-20-OR | 20 (40 μL) | 200 μL |  |
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| KLC2-20-GO | 20 (40 μL) | 200 μL |  |
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| KLC2-20-GR | 20 (40 μL) | 200 μL |  |
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| KLC2-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016]
Gene Symbol : KLC2
Gene Name : Kinesin light chain 2
Chromosome : CHR 11: 662,572,93-662,678,60
Locus : 11q13.2
Alt. Genes : RBM12
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