CLN5 FISH Probe
The CLN5 FISH probe is designed to hybridize to the CLN5 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 |
|---|---|---|---|---|
| CLN5-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| CLN5-20-RE | 20 (40 μL) | 200 μL |  |
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| CLN5-20-GO | 20 (40 μL) | 200 μL |  |
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| CLN5-20-GR | 20 (40 μL) | 200 μL |  |
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| CLN5-20-AQ | 20 (40 μL) | 200 μL |  |
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| CLN5-20-DIG | 20 (40 μL) | 200 μL |  |
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| CLN5-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008]
Gene Details
Gene Symbol: CLN5
Gene Name: CLN5, Intracellular Trafficking Protein
Chromosome: CHR13: 77566058-77576652
Locus: 13q22.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: CLN5 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: CLN5-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping