PGM1-SLC16A12 Fusion FISH Probe
The PGM1-SLC16A12 Fusion FISH Probe is used to confirm a fusion of the PGM1 and SLC16A12 genes. The fusion of the PGM1 and SLC16A12 genes has been associated with Prostate Adenocarcinoma. 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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| PGM1-SLC16A12-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-RERE | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-REOR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-REGO | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-REGR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-REAQ | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-ORRE | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-OROR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-ORGO | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-ORAQ | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GORE | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GOOR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GOGO | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GOGR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GOAQ | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GRRE | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GROR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GRGO | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GRGR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-GRAQ | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-AQRE | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-AQOR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-AQGO | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-AQGR | 20 (40 μL) | 200 μL |
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| PGM1-SLC16A12-20-AQAQ | 20 (40 μL) | 200 μL |
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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
SLC16A12 Gene Summary
This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]
Gene Name: Solute Carrier Family 16 Member 12
Chromosome: CHR10: 91190050 -91295313
Locus: 10q23.31
Gene Diseases
The PGM1 SLC16A12 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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