CKAP2L Break Apart FISH Probe
Empire Genomics’ CKAP2L Break Apart FISH Probe is designed to flank the CKAP2L gene and is typically used for detecting CKAP2L rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CKAP2LBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-AQOR | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-GOGR | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-GORE | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-GRGO | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-GRRE | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-ORGR | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-REGO | 20 (40 μL) | 200 μL |
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| CKAP2LBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
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]
Gene Details
Gene Symbol: CKAP2L
Gene Name: Cytoskeleton Associated Protein 2 Like
Chromosome: CHR2: 113495443-113522254
Locus: 2q14.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: CKAP2L FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: CKAP2L-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping