SOX5-MANSC1 Fusion FISH Probe
The SOX5-MANSC1 Fusion FISH Probe is used to confirm a fusion of the SOX5 and MANSC1 genes. The fusion of the SOX5 and MANSC1 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. 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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| SOX5-MANSC1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-RERE | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-REOR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-REGO | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-REGR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-REAQ | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-ORRE | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-OROR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-ORGO | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GORE | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GOOR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GOGO | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GOGR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GRRE | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GROR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GRGO | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GRGR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-AQRE | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-AQOR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-AQGO | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-AQGR | 20 (40 μL) | 200 μL |
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| SOX5-MANSC1-20-AQAQ | 20 (40 μL) | 200 μL |
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SOX5 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 regulator after forming a protein complex with other proteins. The encoded protein may play a role in chondrogenesis. A pseudogene of this gene is located on chromosome 8. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Name: SRY-box 5
Chromosome: CHR12: 23685230 -24715380
Locus: 12p12.1
MANSC1 Gene Summary
The MANSC Domain Containing 1 (MANSC1) gene is located on chr12 :12482217-12503169 at 12p13.2.
Gene Name: MANSC Domain Containing 1
Chromosome: CHR12: 12482217 -12503169
Locus: 12p13.2
Gene Diseases
The SOX5 MANSC1 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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