FKTN Break Apart FISH Probe
Empire Genomics’ FKTN Break Apart FISH Probe is designed to flank the FKTN gene and is typically used for detecting FKTN rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green 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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| FKTNBA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FKTNBA-20-AQOR | 20 (40 μL) | 200 μL |
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| FKTNBA-20-GOGR | 20 (40 μL) | 200 μL |
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| FKTNBA-20-GORE | 20 (40 μL) | 200 μL |
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| FKTNBA-20-GRGO | 20 (40 μL) | 200 μL |
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| FKTNBA-20-GROR | 20 (40 μL) | 200 μL |
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| FKTNBA-20-GRRE | 20 (40 μL) | 200 μL |
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| FKTNBA-20-REGO | 20 (40 μL) | 200 μL |
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| FKTNBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2010]
Gene Details
Gene Symbol: FKTN
Gene Name: Fukutin
Chromosome: CHR9: 108320410-108403399
Locus: 9q31.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FKTN FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FKTN-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping