SOX10-FAM168A Fusion FISH Probe
The SOX10-FAM168A Fusion FISH Probe is used to confirm a fusion of the SOX10 and FAM168A genes. The fusion of the SOX10 and FAM168A genes has been associated with Brain Lower Grade Glioma. 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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| SOX10-FAM168A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-RERE | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-REOR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-REGO | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-REGR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-REAQ | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-ORRE | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-OROR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-ORGO | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-ORAQ | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GORE | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GOOR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GOGO | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GOGR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GOAQ | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GRRE | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GROR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GRGO | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GRGR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-GRAQ | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-AQRE | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-AQOR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-AQGO | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-AQGR | 20 (40 μL) | 200 μL |
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| SOX10-FAM168A-20-AQAQ | 20 (40 μL) | 200 μL |
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SOX10 Gene Summary
This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008]
Gene Name: SRY-box 10
Chromosome: CHR22: 38368318 -38380539
Locus: 22q13.1
FAM168A Gene Summary
The Family With Sequence Similarity 168 Member A (FAM168A) gene is located on chr11 :73117027-73309228 at 11q13.4.
Gene Name: Family With Sequence Similarity 168 Member A
Chromosome: CHR11: 73117027 -73309228
Locus: 11q13.4
Gene Diseases
The SOX10 FAM168A Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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