SLC20A2-ANKH Fusion FISH Probe
The SLC20A2-ANKH Fusion FISH Probe is used to confirm a fusion of the SLC20A2 and ANKH genes. The fusion of the SLC20A2 and ANKH genes has been associated with Head And Neck Squamous 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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| SLC20A2-ANKH-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-RERE | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-REOR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-REGO | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-REGR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-OROR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GORE | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GROR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC20A2-ANKH-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC20A2 Gene Summary
This gene encodes a member of the inorganic phosphate transporter family. The encoded protein is a type 3 sodium-dependent phosphate symporter that plays an important role in phosphate homeostasis by mediating cellular phosphate uptake. The encoded protein also confers susceptibility to viral infection as a gamma-retroviral receptor. Mutations in this gene may play a role in familial idiopathic basal ganglia calcification. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]
Gene Name: Solute Carrier Family 20 Member 2
Chromosome: CHR8: 42273992 -42397068
Locus: 8p11.21
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 SLC20A2 ANKH Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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