SEH1L-IMPA2 Fusion FISH Probe
The SEH1L-IMPA2 Fusion FISH Probe is used to confirm a fusion of the SEH1L and IMPA2 genes. The fusion of the SEH1L and IMPA2 genes has been associated with Pancreatic Adenocarcinoma. 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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| SEH1L-IMPA2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-RERE | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-REOR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-REGO | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-REGR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-REAQ | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-ORRE | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-OROR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-ORGO | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-ORAQ | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GORE | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GOOR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GOGO | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GOGR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GOAQ | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GRRE | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GROR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GRGO | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GRGR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-GRAQ | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-AQRE | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-AQOR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-AQGO | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-AQGR | 20 (40 μL) | 200 μL |
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| SEH1L-IMPA2-20-AQAQ | 20 (40 μL) | 200 μL |
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IMPA2 Gene Summary
This locus encodes an inositol monophosphatase. The encoded protein catalyzes the dephosphoylration of inositol monophosphate and plays an important role in phosphatidylinositol signaling. This locus may be associated with susceptibility to bipolar disorder. [provided by RefSeq, Jan 2011]
Gene Name: Inositol Monophosphatase 2
Chromosome: CHR18: 11981426 -12030885
Locus: 18p11.21
SEH1L Gene Summary
The protein encoded by this gene is part of a nuclear pore complex, Nup107-160. This protein contains WD repeats and shares 34% amino acid identity with yeast Seh1 and 30% identity with yeast Sec13. All constituents of the Nup107-160 complex, including this protein, specifically localize to kinetochores in mitosis. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: SEH1 Like Nucleoporin
Chromosome: CHR18: 12947982 -12987536
Locus: 18p11.21
Gene Diseases
The SEH1L IMPA2 Fusion has been associated with the following diseases:
| Disease Name |
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| Pancreatic Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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