KIAA0240-PMS1 Fusion FISH Probe
The KIAA0240-PMS1 Fusion FISH Probe is used to confirm a fusion of the KIAA0240 and PMS1 genes. The fusion of the KIAA0240 and PMS1 genes has been associated with Kidney Renal Papillary Cell Carcinoma. 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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| KIAA0240-PMS1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-RERE | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-REOR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-REGO | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-REGR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-REAQ | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-ORRE | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-OROR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-ORGO | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-ORAQ | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GORE | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GOOR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GOGO | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GOGR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GOAQ | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GRRE | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GROR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GRGO | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GRGR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-GRAQ | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-AQRE | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-AQOR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-AQGO | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-AQGR | 20 (40 μL) | 200 μL |
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| KIAA0240-PMS1-20-AQAQ | 20 (40 μL) | 200 μL |
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PMS1 Gene Summary
This gene encodes a protein belonging to the DNA mismatch repair mutL/hexB family. This protein is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in this gene cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also known as Lynch syndrome. [provided by RefSeq, Jul 2008]
Gene Name: PMS1 Homolog 1, Mismatch Repair System Component
Chromosome: CHR2: 190648810 -190742355
Locus: 2q32.2
Gene Diseases
The KIAA0240 PMS1 Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Papillary Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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