KCNQ1-LSP1 Fusion FISH Probe
The KCNQ1-LSP1 Fusion FISH Probe is used to confirm a fusion of the KCNQ1 and LSP1 genes. The fusion of the KCNQ1 and LSP1 genes has been associated with Uterine Carcinosarcoma. 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| KCNQ1-LSP1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-RERE | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-REOR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-REGO | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-REGR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-REAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-ORRE | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-OROR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-ORGO | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-ORAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GORE | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GOOR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GOGO | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GOGR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GOAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GRRE | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GROR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GRGO | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GRGR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-GRAQ | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-AQRE | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-AQOR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-AQGO | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-AQGR | 20 (40 μL) | 200 μL |
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| KCNQ1-LSP1-20-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
LSP1 Gene Summary
This gene encodes an intracellular F-actin binding protein. The protein is expressed in lymphocytes, neutrophils, macrophages, and endothelium and may regulate neutrophil motility, adhesion to fibrinogen matrix proteins, and transendothelial migration. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Name: Lymphocyte-specific Protein 1
Chromosome: CHR11: 1874199 -1913493
Locus: 11p15.5
Gene Diseases
The KCNQ1 LSP1 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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