RUNX1T1-FAM164A Fusion FISH Probe
The RUNX1T1-FAM164A Fusion FISH Probe is used to confirm a fusion of the RUNX1T1 and FAM164A genes. The fusion of the RUNX1T1 and FAM164A genes has been associated with Esophageal 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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| RUNX1T1-FAM164A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-RERE | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-REOR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-REGO | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-REGR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-REAQ | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-ORRE | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-OROR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-ORGO | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-ORAQ | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GORE | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GOOR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GOGO | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GOGR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GOAQ | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GRRE | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GROR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GRGO | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GRGR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-GRAQ | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-AQRE | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-AQOR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-AQGO | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-AQGR | 20 (40 μL) | 200 μL |
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| RUNX1T1-FAM164A-20-AQAQ | 20 (40 μL) | 200 μL |
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RUNX1T1 Gene Summary
This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]
Gene Name: RUNX1 Translocation Partner 1
Chromosome: CHR8: 92967194 -93115454
Locus: 8q21.3
Gene Diseases
The RUNX1T1 FAM164A Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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