CMD1X FISH Probe
The CMD1X FISH probe is designed to hybridize to the CMD1X gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** 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 |
|---|---|---|---|---|
| FKTN-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| FKTN-20-RE | 20 (40 μL) | 200 μL |  |
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| FKTN-20-GO | 20 (40 μL) | 200 μL |  |
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| FKTN-20-GR | 20 (40 μL) | 200 μL |  |
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| FKTN-20-AQ | 20 (40 μL) | 200 μL |  |
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| FKTN-20-DIG | 20 (40 μL) | 200 μL |  |
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| FKTN-20-BIO | 20 (40 μL) | 200 μL |  |
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: CMD1X 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