MLLT10-KCNJ6 Fusion FISH Probe
The MLLT10-KCNJ6 Fusion FISH Probe is used to confirm a fusion of the MLLT10 and KCNJ6 genes. The fusion of the MLLT10 and KCNJ6 genes has been associated with Lung Adenocarcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** 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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| MLLT10-KCNJ6-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-RERE | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-REOR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-REGO | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-REGR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-REAQ | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-ORRE | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-OROR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-ORGO | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-ORAQ | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GORE | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GOOR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GOGO | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GOGR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GOAQ | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GRRE | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GROR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GRGO | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GRGR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-GRAQ | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-AQRE | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-AQOR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-AQGO | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-AQGR | 20 (40 μL) | 200 μL |
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| MLLT10-KCNJ6-20-AQAQ | 20 (40 μL) | 200 μL |
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KCNJ6 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 Name: Potassium Voltage-gated Channel Subfamily J Member 6
Chromosome: CHR21: 38996785 -39288696
Locus: 21q22.13
MLLT10 Gene Summary
This gene encodes a transcription factor and has been identified as a partner gene involved in several chromosomal rearrangements resulting in various leukemias. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]
Gene Name: MLLT10, Histone Lysine Methyltransferase DOT1L Cofactor
Chromosome: CHR10: 21823100 -22032559
Locus: 10p12.31
Gene Diseases
The MLLT10 KCNJ6 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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