PGD-NTSR1 Fusion FISH Probe
The PGD-NTSR1 Fusion FISH Probe is used to confirm a fusion of the PGD and NTSR1 genes. The fusion of the PGD and NTSR1 genes has been associated with Lung Squamous Cell Carcinoma. 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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| PGD-NTSR1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-RERE | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-REOR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-REGO | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-REGR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-REAQ | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-ORRE | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-OROR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-ORGO | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-ORAQ | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GORE | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GOOR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GOGO | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GOGR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GOAQ | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GRRE | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GROR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GRGO | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GRGR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-GRAQ | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-AQRE | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-AQOR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-AQGO | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-AQGR | 20 (40 μL) | 200 μL |
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| PGD-NTSR1-20-AQAQ | 20 (40 μL) | 200 μL |
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NTSR1 Gene Summary
Neurotensin receptor 1 belongs to the large superfamily of G-protein coupled receptors. NTSR1 mediates the multiple functions of neurotensin, such as hypotension, hyperglycemia, hypothermia, antinociception, and regulation of intestinal motility and secretion. [provided by RefSeq, Jul 2008]
Gene Name: Neurotensin Receptor 1
Chromosome: CHR20: 61340188 -61394123
Locus: 20q13.33
PGD Gene Summary
6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]
Gene Name: Phosphogluconate Dehydrogenase
Chromosome: CHR1: 10459084 -10480201
Locus: 1p36.22
Gene Diseases
The PGD NTSR1 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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