BHLHE41-RERGL Fusion FISH Probe
The BHLHE41-RERGL Fusion FISH Probe is used to confirm a fusion of the BHLHE41 and RERGL genes. The fusion of the BHLHE41 and RERGL 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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| BHLHE41-RERGL-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-RERE | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-REOR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-REGO | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-REGR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-REAQ | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-ORRE | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-OROR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-ORGO | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-ORAQ | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GORE | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GOOR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GOGO | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GOGR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GOAQ | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GRRE | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GROR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GRGO | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GRGR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-GRAQ | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-AQRE | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-AQOR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-AQGO | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-AQGR | 20 (40 μL) | 200 μL |
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| BHLHE41-RERGL-20-AQAQ | 20 (40 μL) | 200 μL |
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BHLHE41 Gene Summary
This gene encodes a basic helix-loop-helix protein expressed in various tissues. The encoded protein can interact with ARNTL or compete for E-box binding sites in the promoter of PER1 and repress CLOCK/ARNTL's transactivation of PER1. This gene is believed to be involved in the control of circadian rhythm and cell differentiation. Defects in this gene are associated with the short sleep phenotype. [provided by RefSeq, Feb 2014]
Gene Name: Basic Helix-loop-helix Family Member E41
Chromosome: CHR12: 26272958 -26278003
Locus: 12p12.1
RERGL Gene Summary
The RERG Like (RERGL) gene is located on chr12 :18233802-18243114 at 12p12.3.
Gene Name: RERG Like
Chromosome: CHR12: 18233802 -18243114
Locus: 12p12.3
Gene Diseases
The BHLHE41 RERGL 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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