XPNPEP1-FAM13B Fusion FISH Probe
The XPNPEP1-FAM13B Fusion FISH Probe is used to confirm a fusion of the XPNPEP1 and FAM13B genes. The fusion of the XPNPEP1 and FAM13B 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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| XPNPEP1-FAM13B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-RERE | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-REOR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-REGO | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-REGR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-REAQ | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-ORRE | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-OROR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-ORGO | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-ORAQ | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GORE | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GOOR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GOGO | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GOGR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GOAQ | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GRRE | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GROR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GRGO | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GRGR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-GRAQ | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-AQRE | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-AQOR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-AQGO | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-AQGR | 20 (40 μL) | 200 μL |
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| XPNPEP1-FAM13B-20-AQAQ | 20 (40 μL) | 200 μL |
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XPNPEP1 Gene Summary
This gene encodes the cytosolic form of a metalloaminopeptidase that catalyzes the cleavage of the N-terminal amino acid adjacent to a proline residue. The gene product may play a role in degradation and maturation of tachykinins, neuropeptides, and peptide hormones. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Nov 2009]
Gene Name: X-prolyl Aminopeptidase 1
Chromosome: CHR10: 111624523 -111683311
Locus: 10q25.1
FAM13B Gene Summary
The Family With Sequence Similarity 13 Member B (FAM13B) gene is located on chr5 :137273641-137368802 at 5q31.2.
Gene Name: Family With Sequence Similarity 13 Member B
Chromosome: CHR5: 137273641 -137368802
Locus: 5q31.2
Gene Diseases
The XPNPEP1 FAM13B 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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