PGM1-CHN1 Fusion FISH Probe
The PGM1-CHN1 Fusion FISH Probe is used to confirm a fusion of the PGM1 and CHN1 genes. The fusion of the PGM1 and CHN1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PGM1-CHN1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-RERE | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-REOR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-REGO | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-REGR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-OROR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GORE | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GROR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| PGM1-CHN1-20-AQAQ | 20 (40 μL) | 200 μL |
|
CHN1 Gene Summary
This gene encodes GTPase-activating protein for ras-related p21-rac and a phorbol ester receptor. It is predominantly expressed in neurons, and plays an important role in neuronal signal-transduction mechanisms. Mutations in this gene are associated with Duane's retraction syndrome 2 (DURS2). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011]
Gene Name: Chimerin 1
Chromosome: CHR2: 175664041 -175870107
Locus: 2q31.1
PGM1 Gene Summary
The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90% of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Mar 2010]
Gene Name: Phosphoglucomutase 1
Chromosome: CHR1: 64058946 -64125916
Locus: 1p31.3
Gene Diseases
The PGM1 CHN1 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Mesothelioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|