ITPA-SLC22A24 Fusion FISH Probe
The ITPA-SLC22A24 Fusion FISH Probe is used to confirm a fusion of the ITPA and SLC22A24 genes. The fusion of the ITPA and SLC22A24 genes has been associated with Breast Invasive 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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| ITPA-SLC22A24-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-RERE | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-REOR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-REGO | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-REGR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-REAQ | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-ORRE | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-OROR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-ORGO | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-ORAQ | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GORE | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GOOR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GOGO | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GOGR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GOAQ | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GRRE | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GROR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GRGO | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GRGR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-GRAQ | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-AQRE | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-AQOR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-AQGO | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-AQGR | 20 (40 μL) | 200 μL |
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| ITPA-SLC22A24-20-AQAQ | 20 (40 μL) | 200 μL |
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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
SLC22A24 Gene Summary
SLC22A24 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]
Gene Name: Solute Carrier Family 22 Member 24
Chromosome: CHR11: 62847411 -62911693
Locus: 11q12.3
Gene Diseases
The ITPA SLC22A24 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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