AMPD3-ANKH Fusion FISH Probe
The AMPD3-ANKH Fusion FISH Probe is used to confirm a fusion of the AMPD3 and ANKH genes. The fusion of the AMPD3 and ANKH 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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| AMPD3-ANKH-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-RERE | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-REOR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-REGO | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-REGR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-REAQ | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-ORRE | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-OROR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-ORGO | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-ORAQ | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GORE | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GOOR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GOGO | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GOGR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GOAQ | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GRRE | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GROR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GRGO | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GRGR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-GRAQ | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-AQRE | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-AQOR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-AQGO | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-AQGR | 20 (40 μL) | 200 μL |
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| AMPD3-ANKH-20-AQAQ | 20 (40 μL) | 200 μL |
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AMPD3 Gene Summary
This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jul 2008]
Gene Name: Adenosine Monophosphate Deaminase 3
Chromosome: CHR11: 10471867 -10529126
Locus: 11p15.4
ANKH Gene Summary
This gene encodes a multipass transmembrane protein that is expressed in joints and other tissues and controls pyrophosphate levels in cultured cells. Progressive ankylosis-mediated control of pyrophosphate levels has been suggested as a possible mechanism regulating tissue calcification and susceptibility to arthritis in higher animals. Mutations in this gene have been associated with autosomal dominant craniometaphyseal dysplasia. [provided by RefSeq, Jul 2008]
Gene Name: ANKH Inorganic Pyrophosphate Transport Regulator
Chromosome: CHR5: 14704908 -14871887
Locus: 5p15.2
Gene Diseases
The AMPD3 ANKH 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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