CHGB-IGF2 Fusion FISH Probe
The CHGB-IGF2 Fusion FISH Probe is used to confirm a fusion of the CHGB and IGF2 genes. The fusion of the CHGB and IGF2 genes has been associated with Pheochromocytoma And Paraganglioma, Pheochromocytoma And Paraganglioma, and Pheochromocytoma And Paraganglioma. 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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| CHGB-IGF2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-RERE | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-REOR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-REGO | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-REGR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-REAQ | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-ORRE | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-OROR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-ORGO | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-ORAQ | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GORE | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GOOR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GOGO | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GOGR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GOAQ | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GRRE | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GROR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GRGO | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GRGR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-GRAQ | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-AQRE | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-AQOR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-AQGO | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-AQGR | 20 (40 μL) | 200 μL |
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| CHGB-IGF2-20-AQAQ | 20 (40 μL) | 200 μL |
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CHGB Gene Summary
This gene encodes a tyrosine-sulfated secretory protein abundant in peptidergic endocrine cells and neurons. This protein may serve as a precursor for regulatory peptides. [provided by RefSeq, Jan 2009]
Gene Name: Chromogranin B
Chromosome: CHR20: 5891973 -5906005
Locus: 20p12.3
IGF2 Gene Summary
This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5' region overlaps the INS gene and the 3' region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]
Gene Name: Insulin Like Growth Factor 2
Chromosome: CHR11: 2150346 -2170833
Locus: 11p15.5
Gene Diseases
The CHGB IGF2 Fusion has been associated with the following diseases:
| Disease Name |
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| Pheochromocytoma And Paraganglioma |
| Pheochromocytoma And Paraganglioma |
| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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