RYR2-WLS Fusion FISH Probe
The RYR2-WLS Fusion FISH Probe is used to confirm a fusion of the RYR2 and WLS genes. The fusion of the RYR2 and WLS genes has been associated with Brain Lower Grade Glioma. 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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RYR2-WLS-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-RERE | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-REOR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-REGO | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-REGR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-REAQ | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-ORRE | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-OROR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-ORGO | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-ORAQ | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GORE | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GOOR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GOGO | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GOGR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GOAQ | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GRRE | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GROR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GRGO | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GRGR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-GRAQ | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-AQRE | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-AQOR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-AQGO | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-AQGR | 20 (40 μL) | 200 μL | ||
RYR2-WLS-20-AQAQ | 20 (40 μL) | 200 μL |
RYR2 Gene Summary
This gene encodes a ryanodine receptor found in cardiac muscle sarcoplasmic reticulum. The encoded protein is one of the components of a calcium channel, composed of a tetramer of the ryanodine receptor proteins and a tetramer of FK506 binding protein 1B proteins, that supplies calcium to cardiac muscle. Mutations in this gene are associated with stress-induced polymorphic ventricular tachycardia and arrhythmogenic right ventricular dysplasia. [provided by RefSeq, Jul 2008]
Gene Name: Ryanodine Receptor 2
Chromosome: CHR1: 237205701 -237997288
Locus: 1q43
WLS Gene Summary
The Wntless Wnt Ligand Secretion Mediator (WLS) gene is located on chr1 :68564141-68698229 at 1p31.3.
Gene Name: Wntless Wnt Ligand Secretion Mediator
Chromosome: CHR1: 68564141 -68698229
Locus: 1p31.3
Gene Diseases
The RYR2 WLS Fusion has been associated with the following diseases:
Disease Name |
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Brain Lower Grade Glioma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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