EPS8L2-AGPAT2 Fusion FISH Probe
The EPS8L2-AGPAT2 Fusion FISH Probe is used to confirm a fusion of the EPS8L2 and AGPAT2 genes. The fusion of the EPS8L2 and AGPAT2 genes has been associated with Head And Neck Squamous Cell Carcinoma . 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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| EPS8L2-AGPAT2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-RERE | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-REOR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-REGO | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-REGR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-REAQ | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-ORRE | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-OROR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-ORGO | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-ORAQ | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GORE | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GOOR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GOGO | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GOGR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GOAQ | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GRRE | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GROR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GRGO | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GRGR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-GRAQ | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-AQRE | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-AQOR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-AQGO | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-AQGR | 20 (40 μL) | 200 μL |
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| EPS8L2-AGPAT2-20-AQAQ | 20 (40 μL) | 200 μL |
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AGPAT2 Gene Summary
This gene encodes a member of the 1-acylglycerol-3-phosphate O-acyltransferase family. The protein is located within the endoplasmic reticulum membrane and converts lysophosphatidic acid to phosphatidic acid, the second step in de novo phospholipid biosynthesis. Mutations in this gene have been associated with congenital generalized lipodystrophy (CGL), or Berardinelli-Seip syndrome, a disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Gene Name: 1-acylglycerol-3-phosphate O-acyltransferase 2
Chromosome: CHR9: 139567594 -139581911
Locus: 9q34.3
EPS8L2 Gene Summary
This gene encodes a member of the EPS8 gene family. The encoded protein, like other members of the family, is thought to link growth factor stimulation to actin organization, generating functional redundancy in the pathways that regulate actin cytoskeletal remodeling. [provided by RefSeq, Dec 2008]
Gene Name: EPS8 Like 2
Chromosome: CHR11: 706119 -727727
Locus: 11p15.5
Gene Diseases
The EPS8L2 AGPAT2 Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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