PLEKHF1-C19ORF12 Fusion FISH Probe
The PLEKHF1-C19ORF12 Fusion FISH Probe is used to confirm a fusion of the PLEKHF1 and C19ORF12 genes. The fusion of the PLEKHF1 and C19ORF12 genes has been associated with Stomach Adenocarcinoma. 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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| PLEKHF1-C19ORF12-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-RERE | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-REOR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-REGO | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-REGR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-REAQ | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-ORRE | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-OROR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-ORGO | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-ORAQ | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GORE | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GOOR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GOGO | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GOGR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GOAQ | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GRRE | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GROR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GRGO | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GRGR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-GRAQ | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-AQRE | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-AQOR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-AQGO | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-AQGR | 20 (40 μL) | 200 μL |
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| PLEKHF1-C19ORF12-20-AQAQ | 20 (40 μL) | 200 μL |
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PLEKHF1 Gene Summary
The Pleckstrin Homology And FYVE Domain Containing 1 (PLEKHF1) gene is located on chr19 :30156326-30166383 at 19q12.
Gene Name: Pleckstrin Homology And FYVE Domain Containing 1
Chromosome: CHR19: 30156326 -30166383
Locus: 19q12
C19orf12 Gene Summary
This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Gene Name: Chromosome 19 Open Reading Frame 12
Chromosome: CHR19: 30189792 -30206452
Locus: 19q12
Gene Diseases
The PLEKHF1 C19ORF12 Fusion has been associated with the following diseases:
| Disease Name |
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| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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