SLC44A2-PTPRQ Fusion FISH Probe
The SLC44A2-PTPRQ Fusion FISH Probe is used to confirm a fusion of the SLC44A2 and PTPRQ genes. The fusion of the SLC44A2 and PTPRQ genes has been associated with Sarcoma. 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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| SLC44A2-PTPRQ-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-RERE | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-REOR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-REGO | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-REGR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-OROR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GORE | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GROR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC44A2-PTPRQ-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC44A2 Gene Summary
The Solute Carrier Family 44 Member 2 (SLC44A2) gene is located on chr19 :10713120-10755235 at 19p13.2.
Gene Name: Solute Carrier Family 44 Member 2
Chromosome: CHR19: 10713120 -10755235
Locus: 19p13.2
PTPRQ Gene Summary
This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus have been linked to autosomal recessive deafness. [provided by RefSeq, Mar 2014]
Gene Name: Protein Tyrosine Phosphatase, Receptor Type Q
Chromosome: CHR12: 80838125 -81073968
Locus: 12q21.31
Gene Diseases
The SLC44A2 PTPRQ Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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