CADPS2-RPGR Fusion FISH Probe
The CADPS2-RPGR Fusion FISH Probe is used to confirm a fusion of the CADPS2 and RPGR genes. The fusion of the CADPS2 and RPGR genes has been associated with Cervical Squamous Cell Carcinoma And Endocervical 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CADPS2-RPGR-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-RERE | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-REOR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-REGO | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-REGR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-REAQ | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-ORRE | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-OROR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-ORGO | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-ORAQ | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GORE | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GOOR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GOGO | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GOGR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GOAQ | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GRRE | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GROR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GRGO | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GRGR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-GRAQ | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-AQRE | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-AQOR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-AQGO | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-AQGR | 20 (40 μL) | 200 μL |
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| CADPS2-RPGR-20-AQAQ | 20 (40 μL) | 200 μL |
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RPGR Gene Summary
This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. The encoded protein is found in the Golgi body and interacts with RPGRIP1. This protein localizes to the outer segment of rod photoreceptors and is essential for their viability. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined. [provided by RefSeq, Dec 2008]
Gene Name: Retinitis Pigmentosa GTPase Regulator
Chromosome: CHRX: 38128422 -38186788
Locus: Xp11.4
CADPS2 Gene Summary
This gene encodes a member of the calcium-dependent activator of secretion (CAPS) protein family, which are calcium binding proteins that regulate the exocytosis of synaptic and dense-core vesicles in neurons and neuroendocrine cells. Mutations in this gene may contribute to autism susceptibility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2009]
Gene Name: Calcium Dependent Secretion Activator 2
Chromosome: CHR7: 121958477 -122526813
Locus: 7q31.32
Gene Diseases
The CADPS2 RPGR Fusion has been associated with the following diseases:
| Disease Name |
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| Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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