CLN5 Break Apart FISH Probe
Empire Genomics’ CLN5 Break Apart FISH Probe is designed to flank the CLN5 gene and is typically used for detecting CLN5 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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| CLN5BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CLN5BA-20-AQOR | 20 (40 μL) | 200 μL |
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| CLN5BA-20-GOGR | 20 (40 μL) | 200 μL |
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| CLN5BA-20-GORE | 20 (40 μL) | 200 μL |
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| CLN5BA-20-GRGO | 20 (40 μL) | 200 μL |
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| CLN5BA-20-GROR | 20 (40 μL) | 200 μL |
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| CLN5BA-20-GRRE | 20 (40 μL) | 200 μL |
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| CLN5BA-20-REGO | 20 (40 μL) | 200 μL |
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| CLN5BA-20-REGR | 20 (40 μL) | 200 μL |
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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