CP-WWTR1 Fusion FISH Probe
The CP-WWTR1 Fusion FISH Probe is used to confirm a fusion of the CP and WWTR1 genes. The fusion of the CP and WWTR1 genes has been associated with Breast Invasive 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. 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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| CP-WWTR1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-RERE | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-REOR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-REGO | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-REGR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-REAQ | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-ORRE | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-OROR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-ORGO | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-ORAQ | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GORE | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GOOR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GOGO | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GOGR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GOAQ | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GRRE | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GROR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GRGO | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GRGR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-GRAQ | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-AQRE | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-AQOR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-AQGO | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-AQGR | 20 (40 μL) | 200 μL |
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| CP-WWTR1-20-AQAQ | 20 (40 μL) | 200 μL |
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CP Gene Summary
The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Feb 2012]
Gene Name: Ceruloplasmin
Chromosome: CHR3: 148890289 -148939832
Locus: 3q24-q25.1
WWTR1 Gene Summary
The WW Domain Containing Transcription Regulator 1 (WWTR1) gene is located on chr3 :149235021-149421060 at 3q25.1.
Gene Name: WW Domain Containing Transcription Regulator 1
Chromosome: CHR3: 149235021 -149421060
Locus: 3q25.1
Gene Diseases
The CP WWTR1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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