MEGF8-ITPKC Fusion FISH Probe
The MEGF8-ITPKC Fusion FISH Probe is used to confirm a fusion of the MEGF8 and ITPKC genes. The fusion of the MEGF8 and ITPKC genes has been associated with Sarcoma. 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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| MEGF8-ITPKC-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-RERE | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-REOR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-REGO | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-REGR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-REAQ | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-ORRE | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-OROR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-ORGO | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-ORAQ | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GORE | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GOOR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GOGO | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GOGR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GOAQ | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GRRE | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GROR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GRGO | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GRGR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-GRAQ | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-AQRE | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-AQOR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-AQGO | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-AQGR | 20 (40 μL) | 200 μL |
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| MEGF8-ITPKC-20-AQAQ | 20 (40 μL) | 200 μL |
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MEGF8 Gene Summary
The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
Gene Name: Multiple EGF Like Domains 8
Chromosome: CHR19: 42829760 -42882921
Locus: 19q13.2
ITPKC Gene Summary
This gene encodes a member of the inositol 1,4,5-trisphosphate [Ins(1,4,5)P(3)] 3-kinase family of enzymes that catalyze the phosphorylation of inositol 1,4,5-trisphosphate to 1,3,4,5-tetrakisphosphate. The encoded protein is localized to the nucleus and cytoplasm and has both nuclear import and nuclear export activity. Single nucleotide polymorphisms in this gene are associated with Kawasaki disease.[provided by RefSeq, Sep 2009]
Gene Name: Inositol-trisphosphate 3-kinase C
Chromosome: CHR19: 41223007 -41246765
Locus: 19q13.2
Gene Diseases
The MEGF8 ITPKC Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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