SLC6A5 Break Apart FISH Probe
Empire Genomics’ SLC6A5 Break Apart FISH Probe is designed to flank the SLC6A5 gene and is typically used for detecting SLC6A5 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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| SLC6A5BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-GROR | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC6A5BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia; a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Gene Details
Gene Symbol: SLC6A5
Gene Name: Solute Carrier Family 6 Member 5
Chromosome: CHR11: 20620945-20676610
Locus: 11p15.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC6A5 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC6A5-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping