TRIM2-FAM71F1 Fusion FISH Probe
The TRIM2-FAM71F1 Fusion FISH Probe is used to confirm a fusion of the TRIM2 and FAM71F1 genes. The fusion of the TRIM2 and FAM71F1 genes has been associated with Uterine Corpus Endometrial 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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| TRIM2-FAM71F1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-RERE | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-REOR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-REGO | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-REGR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-REAQ | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-ORRE | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-OROR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-ORGO | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-ORAQ | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GORE | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GOOR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GOGO | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GOGR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GOAQ | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GRRE | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GROR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GRGO | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GRGR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-GRAQ | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-AQRE | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-AQOR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-AQGO | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-AQGR | 20 (40 μL) | 200 μL |
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| TRIM2-FAM71F1-20-AQAQ | 20 (40 μL) | 200 μL |
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TRIM2 Gene Summary
The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic filaments. It plays a neuroprotective role and functions as an E3-ubiquitin ligase in proteasome-mediated degradation of target proteins. Mutations in this gene can cause early-onset axonal neuropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]
Gene Name: Tripartite Motif Containing 2
Chromosome: CHR4: 154074269 -154260474
Locus: 4q31.3
FAM71F1 Gene Summary
The Family With Sequence Similarity 71 Member F1 (FAM71F1) gene is located on chr7 :128355442-128371797 at 7q32.1.
Gene Name: Family With Sequence Similarity 71 Member F1
Chromosome: CHR7: 128355442 -128371797
Locus: 7q32.1
Gene Diseases
The TRIM2 FAM71F1 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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