KCNQ1-GALNTL6 Fusion FISH Probe
The KCNQ1-GALNTL6 Fusion FISH Probe is used to confirm a fusion of the KCNQ1 and GALNTL6 genes. The fusion of the KCNQ1 and GALNTL6 genes has been associated with Colon 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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| KCNQ1-GALNTL6-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-RERE | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-REOR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-REGO | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-REGR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-REAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-ORRE | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-OROR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-ORGO | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-ORAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GORE | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GOOR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GOGO | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GOGR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GOAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GRRE | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GROR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GRGO | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GRGR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-GRAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-AQRE | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-AQOR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-AQGO | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-AQGR | 20 (40 μL) | 200 μL |
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| KCNQ1-GALNTL6-20-AQAQ | 20 (40 μL) | 200 μL |
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KCNQ1 Gene Summary
This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011]
Gene Name: Potassium Voltage-gated Channel Subfamily Q Member 1
Chromosome: CHR11: 2466220 -2870340
Locus: 11p15.5-p15.4
GALNTL6 Gene Summary
The Polypeptide N-acetylgalactosaminyltransferase Like 6 (GALNTL6) gene is located on chr4 :172734574-173961558 at 4q34.1.
Gene Name: Polypeptide N-acetylgalactosaminyltransferase Like 6
Chromosome: CHR4: 172734574 -173961558
Locus: 4q34.1
Gene Diseases
The KCNQ1 GALNTL6 Fusion has been associated with the following diseases:
| Disease Name |
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| Colon Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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