POMT1-PPAPDC3 Fusion FISH Probe
The POMT1-PPAPDC3 Fusion FISH Probe is used to confirm a fusion of the POMT1 and PPAPDC3 genes. The fusion of the POMT1 and PPAPDC3 genes has been associated with Liver Hepatocellular 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. 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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| POMT1-PPAPDC3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-RERE | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-REOR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-REGO | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-REGR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-REAQ | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-ORRE | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-OROR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-ORGO | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-ORAQ | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GORE | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GOOR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GOGO | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GOGR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GOAQ | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GRRE | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GROR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GRGO | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GRGR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-GRAQ | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-AQRE | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-AQOR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-AQGO | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-AQGR | 20 (40 μL) | 200 μL |
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| POMT1-PPAPDC3-20-AQAQ | 20 (40 μL) | 200 μL |
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POMT1 Gene Summary
The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2008]
Gene Name: Protein O-mannosyltransferase 1
Chromosome: CHR9: 134378288 -134399193
Locus: 9q34.13
Gene Diseases
The POMT1 PPAPDC3 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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