MSH2-SLCO6A1 Fusion FISH Probe
The MSH2-SLCO6A1 Fusion FISH Probe is used to confirm a fusion of the MSH2 and SLCO6A1 genes. The fusion of the MSH2 and SLCO6A1 genes has been associated with 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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| MSH2-SLCO6A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-RERE | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-REOR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-REGO | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-REGR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-REAQ | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-ORRE | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-OROR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-ORGO | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GORE | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GOOR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GOGO | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GOGR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GRRE | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GROR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GRGO | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GRGR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-AQRE | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-AQOR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-AQGO | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-AQGR | 20 (40 μL) | 200 μL |
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| MSH2-SLCO6A1-20-AQAQ | 20 (40 μL) | 200 μL |
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MSH2 Gene Summary
This locus is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Gene Name: MutS Homolog 2
Chromosome: CHR2: 47630262 -47710360
Locus: 2p21-p16.3
SLCO6A1 Gene Summary
The Solute Carrier Organic Anion Transporter Family Member 6A1 (SLCO6A1) gene is located on chr5 :101707651-101834720 at 5q21.1.
Gene Name: Solute Carrier Organic Anion Transporter Family Member 6A1
Chromosome: CHR5: 101707651 -101834720
Locus: 5q21.1
Gene Diseases
The MSH2 SLCO6A1 Fusion has been associated with the following diseases:
| Disease Name |
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| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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