C21ORF56-IGF1 Fusion FISH Probe
The C21ORF56-IGF1 Fusion FISH Probe is used to confirm a fusion of the C21ORF56 and IGF1 genes. The fusion of the C21ORF56 and IGF1 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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| C21ORF56-IGF1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-RERE | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-REOR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-REGO | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-REGR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-REAQ | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-ORRE | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-OROR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-ORGO | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-ORAQ | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GORE | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GOOR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GOGO | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GOGR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GOAQ | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GRRE | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GROR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GRGO | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GRGR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-GRAQ | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-AQRE | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-AQOR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-AQGO | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-AQGR | 20 (40 μL) | 200 μL |
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| C21ORF56-IGF1-20-AQAQ | 20 (40 μL) | 200 μL |
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IGF1 Gene Summary
The protein encoded by this gene is similar to insulin in function and structure and is a member of a family of proteins involved in mediating growth and development. The encoded protein is processed from a precursor, bound by a specific receptor, and secreted. Defects in this gene are a cause of insulin-like growth factor I deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015]
Gene Name: Insulin Like Growth Factor 1
Chromosome: CHR12: 102789644 -102874378
Locus: 12q23.2
Gene Diseases
The C21ORF56 IGF1 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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