FAM169A-ANKRD31 Fusion FISH Probe
The FAM169A-ANKRD31 Fusion FISH Probe is used to confirm a fusion of the FAM169A and ANKRD31 genes. The fusion of the FAM169A and ANKRD31 genes has been associated with Bladder Urothelial 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| FAM169A-ANKRD31-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-RERE | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-REOR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-REGO | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-REGR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-OROR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GORE | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GROR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM169A-ANKRD31-20-AQAQ | 20 (40 μL) | 200 μL |
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FAM169A Gene Summary
The Family With Sequence Similarity 169 Member A (FAM169A) gene is located on chr5 :74073398-74162615 at 5q13.3.
Gene Name: Family With Sequence Similarity 169 Member A
Chromosome: CHR5: 74073398 -74162615
Locus: 5q13.3
ANKRD31 Gene Summary
This gene encodes a protein containing multiple ankyrin repeats. Ankyrin domains function in protein-protein interactions in a variety of cellular processes. Mutations in this gene are associated with a Rett syndrome (RTT)-like phenotype. [provided by RefSeq, Apr 2017]
Gene Name: Ankyrin Repeat Domain 31
Chromosome: CHR5: 74364121 -74532703
Locus: 5q13.3
Gene Diseases
The FAM169A ANKRD31 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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