EFCAB4B-C12ORF4 Fusion FISH Probe
The EFCAB4B-C12ORF4 Fusion FISH Probe is used to confirm a fusion of the EFCAB4B and C12ORF4 genes. The fusion of the EFCAB4B and C12ORF4 genes has been associated with Glioblastoma Multiforme. 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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| EFCAB4B-C12ORF4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-RERE | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-REOR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-REGO | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-REGR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-REAQ | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-ORRE | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-OROR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-ORGO | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-ORAQ | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GORE | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GOOR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GOGO | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GOGR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GOAQ | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GRRE | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GROR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GRGO | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GRGR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-GRAQ | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-AQRE | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-AQOR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-AQGO | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-AQGR | 20 (40 μL) | 200 μL |
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| EFCAB4B-C12ORF4-20-AQAQ | 20 (40 μL) | 200 μL |
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C12orf4 Gene Summary
This gene is highly conserved from nematodes to humans. In rat, the orthologous gene encodes a cytoplasmic protein that is involved in mast cell degranulation. The human gene has been implicated in autosomal recessive intellectual disability. [provided by RefSeq, Sep 2016]
Gene Name: Chromosome 12 Open Reading Frame 4
Chromosome: CHR12: 4596900 -4647637
Locus: 12p13.32
Gene Diseases
The EFCAB4B C12ORF4 Fusion has been associated with the following diseases:
| Disease Name |
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| Glioblastoma Multiforme |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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