TMEM5-PTDSS1 Fusion FISH Probe
The TMEM5-PTDSS1 Fusion FISH Probe is used to confirm a fusion of the TMEM5 and PTDSS1 genes. The fusion of the TMEM5 and PTDSS1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| TMEM5-PTDSS1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-RERE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REOR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-ORRE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-OROR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-ORGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-ORAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GORE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOOR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRRE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GROR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQRE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQOR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQAQ | 20 (40 μL) | 200 μL |
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PTDSS1 Gene Summary
The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
Gene Name: Phosphatidylserine Synthase 1
Chromosome: CHR8: 97274166 -97346774
Locus: 8q22.1
TMEM5 Gene Summary
This gene encodes a type II transmembrane protein that is thought to have glycosyltransferase function. Mutations in this gene result in cobblestone lissencephaly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]
Gene Name: Transmembrane Protein 5
Chromosome: CHR12: 64173636 -64202887
Locus: 12q14.2
Gene Diseases
The TMEM5 PTDSS1 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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