LHFPL3-EEA1 Fusion FISH Probe
The LHFPL3-EEA1 Fusion FISH Probe is used to confirm a fusion of the LHFPL3 and EEA1 genes. The fusion of the LHFPL3 and EEA1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| LHFPL3-EEA1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-RERE | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-REOR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-REGO | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-REGR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-REAQ | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-ORRE | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-OROR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-ORGO | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-ORAQ | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GORE | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GOOR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GOGO | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GOGR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GOAQ | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GRRE | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GROR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GRGO | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GRGR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-GRAQ | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-AQRE | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-AQOR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-AQGO | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-AQGR | 20 (40 μL) | 200 μL |
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| LHFPL3-EEA1-20-AQAQ | 20 (40 μL) | 200 μL |
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EEA1 Gene Summary
The Early Endosome Antigen 1 (EEA1) gene is located on chr12 :93166284-93323107 at 12q22.
Gene Name: Early Endosome Antigen 1
Chromosome: CHR12: 93166284 -93323107
Locus: 12q22
LHFPL3 Gene Summary
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. A partial gene fragment named LHFPL4 corresponds to a portion of the first exon of this gene. [provided by RefSeq, Jul 2008]
Gene Name: LHFPL Tetraspan Subfamily Member 3
Chromosome: CHR7: 103969103 -104549003
Locus: 7q22.2-q22.3
Gene Diseases
The LHFPL3 EEA1 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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