The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Apr 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KIF1ABA-20-REGO | 20 (40 μL) | 200 μL |
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| KIF1ABA-20-REGR | 20 (40 μL) | 200 μL |
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| KIF1ABA-20-ORGR | 20 (40 μL) | 200 μL |
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| KIF1ABA-20-GOGR | 20 (40 μL) | 200 μL |
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| KIF1ABA-20-GRRE | 20 (40 μL) | 200 μL |
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| KIF1ABA-20-GROR | 20 (40 μL) | 200 μL |
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| KIF1ABA-20-GRGO | 20 (40 μL) | 200 μL |
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| KIF1ABA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a member of the kinesin family and functions as an anterograde motor protein that transports membranous organelles along axonal microtubules. Mutations at this locus have been associated with spastic paraplegia-30 and hereditary sensory neuropathy IIC. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Apr 2012]
Gene Symbol : KIF1A
Gene Name : Kinesin family member 1A
Chromosome : CHR 2: 240,821,024-240,713,763
Locus : 2q37.3
Alt. Genes : AKAP9
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