SUZ12-VANGL1 Fusion FISH Probe
The SUZ12-VANGL1 Fusion FISH Probe is used to confirm a fusion of the SUZ12 and VANGL1 genes. The fusion of the SUZ12 and VANGL1 genes has been associated with Skin Cutaneous Melanoma. 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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| SUZ12-VANGL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-RERE | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-REOR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-REGO | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-REGR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-REAQ | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-ORRE | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-OROR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-ORGO | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GORE | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GOOR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GOGO | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GOGR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GRRE | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GROR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GRGO | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GRGR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-AQRE | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-AQOR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-AQGO | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-AQGR | 20 (40 μL) | 200 μL |
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| SUZ12-VANGL1-20-AQAQ | 20 (40 μL) | 200 μL |
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SUZ12 Gene Summary
This zinc finger gene has been identified at the breakpoints of a recurrent chromosomal translocation reported in endometrial stromal sarcoma. Recombination of these breakpoints results in the fusion of this gene and JAZF1. The protein encoded by this gene contains a zinc finger domain in the C terminus of the coding region. [provided by RefSeq, Jul 2009]
Gene Name: SUZ12 Polycomb Repressive Complex 2 Subunit
Chromosome: CHR17: 30264043 -30328057
Locus: 17q11.2
VANGL1 Gene Summary
This gene encodes a member of the tretraspanin family. The encoded protein may be involved in mediating intestinal trefoil factor induced wound healing in the intestinal mucosa. Mutations in this gene are associated with neural tube defects. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
Gene Name: VANGL Planar Cell Polarity Protein 1
Chromosome: CHR1: 116184573 -116240845
Locus: 1p13.1
Gene Diseases
The SUZ12 VANGL1 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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