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CKAP2L


Official Full Name
cytoskeleton associated protein 2 like
Organism
Homo sapiens
Gene ID
150468
Background
The protein encoded by this gene is thought to be a mitotic spindle protein important to neural stem or progenitor cells. Mutations in this gene have been associated with spindle organization defects, including mitotic spindle defects, lagging chromosomes, and chromatin bridges. There is evidence that mutations in this gene are associated with Filippi syndrome, characterized by growth defects, microcephaly, intellectual disability, facial feature defects, and syndactyly. There is a pseudogene of this gene on chromosome 20. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]

Cat.No. Product Name Price
SHH264317 shRNA set against Human CKAP2L (NM_152515.3) Inquiry
SHH264321 shRNA set against Mouse CKAP2L (NM_181589.3) Inquiry
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MiUTR1H-02174 CKAP2L miRNA 3'UTR clone Inquiry
CDCB182582 Rabbit CKAP2L ORF clone (XM_002709599.2) Inquiry
CDCR047420 Human CKAP2L ORF clone (NM_152515.3) Inquiry
CDCR275610 Mouse Ckap2l ORF Clone(NM_181589.3) Inquiry
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