RP2-CHST7 Fusion FISH Probe
The RP2-CHST7 Fusion FISH Probe is used to confirm a fusion of the RP2 and CHST7 genes. The fusion of the RP2 and CHST7 genes has been associated with Skin Cutaneous Melanoma. 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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| RP2-CHST7-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-RERE | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-REOR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-REGO | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-REGR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-REAQ | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-ORRE | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-OROR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-ORGO | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-ORAQ | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GORE | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GOOR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GOGO | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GOGR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GOAQ | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GRRE | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GROR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GRGO | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GRGR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-GRAQ | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-AQRE | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-AQOR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-AQGO | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-AQGR | 20 (40 μL) | 200 μL |
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| RP2-CHST7-20-AQAQ | 20 (40 μL) | 200 μL |
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RP2 Gene Summary
The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death [provided by RefSeq, Jul 2008]
Gene Name: RP2, ARL3 GTPase Activating Protein
Chromosome: CHRX: 46696346 -46741791
Locus: Xp11.3
CHST7 Gene Summary
This gene is a member of the Gal/GalNAc/GlcNAc (galactose/N-acetylgalactosamine/N-acetylglucosamine) 6-O-sulfotransferase (GST) family. Members of this family encode enzymes that catalyze the specific addition of sulfate groups to distinct hydroxyl and amino groups of carbohydrates. The encoded protein catalyzes the sulfation of 6-hydroxyl group of GalNAc in chondroitin. [provided by RefSeq, Aug 2013]
Gene Name: Carbohydrate Sulfotransferase 7
Chromosome: CHRX: 46433191 -46457838
Locus: Xp11.3
Gene Diseases
The RP2 CHST7 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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