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KIF5A


Official Full Name
kinesin family member 5A
Organism
Homo sapiens
Gene ID
3798
Background
This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene cause autosomal dominant spastic paraplegia 10. [provided by RefSeq, Jul 2008]
Synonyms
NKHC; ALS25; MY050; NEIMY; SPG10; D12S1889

Cat.No. Product Name Price
SHH325347 shRNA set against Human KIF5A (NM_004984.2) Inquiry
SHH325351 shRNA set against Mouse KIF5A (NM_008447.4) Inquiry
SHH325355 shRNA set against Rat KIF5A (NM_212523.1) Inquiry
SHL197274 shRNA set against Rat Kif5a(NM_212523.1) Inquiry
SHL197352 shRNA set against Human KIF5A(NM_004984.2) Inquiry
Cat.No. Product Name Price
CDCR289341 Human KIF5A ORF Clone(NM_004984.2) Inquiry
CDFH009907 Human KIF5A cDNA Clone(NM_004984.2) Inquiry
CDFR015393 Rat Kif5a cDNA Clone(NM_212523.1) Inquiry
MiUTR1H-05315 KIF5A miRNA 3'UTR clone Inquiry
CDCB193883 Rabbit KIF5A ORF clone (XM_002720919.2) Inquiry
CDCR005668 Mouse KIF5A ORF clone(NM_008447.4) Inquiry
CDCR005671 Mouse KIF5A ORF clone(NM_001039000.4) Inquiry
CDCR382170 Rat Kif5a ORF Clone(NM_212523.1) Inquiry
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