KCNJ6 Break Apart FISH Probe
Empire Genomics’ KCNJ6 Break Apart FISH Probe is designed to flank the KCNJ6 gene and is typically used for detecting KCNJ6 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange 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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| KCNJ6BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-AQOR | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GOGR | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GORE | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GRGO | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GRRE | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-ORGR | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-REGO | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015]
Gene Details
Gene Symbol: KCNJ6
Gene Name: Potassium Voltage-gated Channel Subfamily J Member 6
Chromosome: CHR21: 38996785-39288696
Locus: 21q22.13
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: KCNJ6 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: KCNJ6-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping