PRR5L-ITPA Fusion FISH Probe
The PRR5L-ITPA Fusion FISH Probe is used to confirm a fusion of the PRR5L and ITPA genes. The fusion of the PRR5L and ITPA genes has been associated with Uterine Corpus Endometrial 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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PRR5L-ITPA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-RERE | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-REOR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-REGO | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-REGR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-REAQ | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-ORRE | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-OROR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-ORGO | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-ORAQ | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GORE | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GOOR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GOGO | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GOGR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GOAQ | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GRRE | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GROR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GRGO | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GRGR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-GRAQ | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-AQRE | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-AQOR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-AQGO | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-AQGR | 20 (40 μL) | 200 μL | ||
PRR5L-ITPA-20-AQAQ | 20 (40 μL) | 200 μL |
ITPA Gene Summary
This gene encodes an inosine triphosphate pyrophosphohydrolase. The encoded protein hydrolyzes inosine triphosphate and deoxyinosine triphosphate to the monophosphate nucleotide and diphosphate. This protein, which is a member of the HAM1 NTPase protein family, is found in the cytoplasm and acts as a homodimer. Defects in the encoded protein can result in inosine triphosphate pyrophosphorylase deficiency which causes an accumulation of ITP in red blood cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]
Gene Name: Inosine Triphosphatase
Chromosome: CHR20: 3190055 -3204506
Locus: 20p13
PRR5L Gene Summary
The Proline Rich 5 Like (PRR5L) gene is located on chr11 :36317724-36486754 at 11p13-p12.
Gene Name: Proline Rich 5 Like
Chromosome: CHR11: 36317724 -36486754
Locus: 11p13-p12
Gene Diseases
The PRR5L ITPA Fusion has been associated with the following diseases:
Disease Name |
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Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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