ALG9-PDGFD Fusion FISH Probe
The ALG9-PDGFD Fusion FISH Probe is used to confirm a fusion of the ALG9 and PDGFD genes. The fusion of the ALG9 and PDGFD genes has been associated with Mesothelioma. 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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| ALG9-PDGFD-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-RERE | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-REOR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-REGO | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-REGR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-REAQ | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-ORRE | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-OROR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-ORGO | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-ORAQ | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GORE | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GOOR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GOGO | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GOGR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GOAQ | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GRRE | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GROR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GRGO | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GRGR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-GRAQ | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-AQRE | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-AQOR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-AQGO | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-AQGR | 20 (40 μL) | 200 μL |
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| ALG9-PDGFD-20-AQAQ | 20 (40 μL) | 200 μL |
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ALG9 Gene Summary
This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Name: ALG9, Alpha-1,2-mannosyltransferase
Chromosome: CHR11: 111652918 -111742305
Locus: 11q23.1
PDGFD Gene Summary
The protein encoded by this gene is a member of the platelet-derived growth factor family. The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a core motif of eight cysteines, seven of which are found in this factor. This gene product only forms homodimers and, therefore, does not dimerize with the other three family members. It differs from alpha and beta members of this family in having an unusual N-terminal domain, the CUB domain. Two splice variants have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Platelet Derived Growth Factor D
Chromosome: CHR11: 103777913 -104035027
Locus: 11q22.3
Gene Diseases
The ALG9 PDGFD Fusion has been associated with the following diseases:
| Disease Name |
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| Mesothelioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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