PLEKHM2-TMEM51 Fusion FISH Probe
The PLEKHM2-TMEM51 Fusion FISH Probe is used to confirm a fusion of the PLEKHM2 and TMEM51 genes. The fusion of the PLEKHM2 and TMEM51 genes has been associated with Glioblastoma Multiforme. 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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| PLEKHM2-TMEM51-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-RERE | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-REOR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-REGO | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-REGR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-REAQ | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-ORRE | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-OROR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-ORGO | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-ORAQ | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GORE | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GOOR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GOGO | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GOGR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GOAQ | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GRRE | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GROR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GRGO | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GRGR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-GRAQ | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-AQRE | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-AQOR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-AQGO | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-AQGR | 20 (40 μL) | 200 μL |
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| PLEKHM2-TMEM51-20-AQAQ | 20 (40 μL) | 200 μL |
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PLEKHM2 Gene Summary
This gene encodes a protein that binds the plus-end directed microtubule motor protein kinesin, together with the lysosomal GTPase Arl8, and is required for lysosomes to distribute away from the microtubule-organizing center. The encoded protein belongs to the multisubunit BLOC-one-related complex that regulates lysosome positioning. It binds a Salmonella effector protein called Salmonella induced filament A and is a critical host determinant in Salmonella pathogenesis. It has a domain architecture consisting of an N-terminal RPIP8, UNC-14, and NESCA (RUN) domain that binds kinesin-1 as well as the lysosomal GTPase Arl8, and a C-terminal pleckstrin homology domain that binds the Salmonella induced filament A effector protein. Naturally occurring mutations in this gene lead to abnormal localization of lysosomes, impaired autophagy flux and are associated with recessive dilated cardiomyopathy and left ventricular noncompaction. [provided by RefSeq, Feb 2017]
Gene Name: Pleckstrin Homology And RUN Domain Containing M2
Chromosome: CHR1: 16010826 -16061264
Locus: 1p36.21
TMEM51 Gene Summary
The Transmembrane Protein 51 (TMEM51) gene is located on chr1 :15479027-15546974 at 1p36.21.
Gene Name: Transmembrane Protein 51
Chromosome: CHR1: 15479027 -15546974
Locus: 1p36.21
Gene Diseases
The PLEKHM2 TMEM51 Fusion has been associated with the following diseases:
| Disease Name |
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| Glioblastoma Multiforme |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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