ABCD3-DPYD Fusion FISH Probe
The ABCD3-DPYD Fusion FISH Probe is used to confirm a fusion of the ABCD3 and DPYD genes. The fusion of the ABCD3 and DPYD genes has been associated with Prostate 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. 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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| ABCD3-DPYD-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-RERE | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-REOR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-REGO | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-REGR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-REAQ | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-ORRE | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-OROR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-ORGO | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-ORAQ | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GORE | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GOOR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GOGO | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GOGR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GOAQ | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GRRE | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GROR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GRGO | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GRGR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-GRAQ | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-AQRE | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-AQOR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-AQGO | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-AQGR | 20 (40 μL) | 200 μL |
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| ABCD3-DPYD-20-AQAQ | 20 (40 μL) | 200 μL |
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DPYD Gene Summary
The protein encoded by this gene is a pyrimidine catabolic enzyme and the initial and rate-limiting factor in the pathway of uracil and thymidine catabolism. Mutations in this gene result in dihydropyrimidine dehydrogenase deficiency, an error in pyrimidine metabolism associated with thymine-uraciluria and an increased risk of toxicity in cancer patients receiving 5-fluorouracil chemotherapy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Gene Name: Dihydropyrimidine Dehydrogenase
Chromosome: CHR1: 97543299 -98386615
Locus: 1p21.3
ABCD3 Gene Summary
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
Gene Name: ATP Binding Cassette Subfamily D Member 3
Chromosome: CHR1: 94883932 -94984219
Locus: 1p21.3
Gene Diseases
The ABCD3 DPYD Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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