ATG2B-SLC22A17 Fusion FISH Probe
The ATG2B-SLC22A17 Fusion FISH Probe is used to confirm a fusion of the ATG2B and SLC22A17 genes. The fusion of the ATG2B and SLC22A17 genes has been associated with Bladder Urothelial 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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| ATG2B-SLC22A17-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-RERE | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-REOR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-REGO | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-REGR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-REAQ | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-ORRE | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-OROR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-ORGO | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GORE | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GOOR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GOGO | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GOGR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GRRE | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GROR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GRGO | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GRGR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-AQRE | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-AQOR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-AQGO | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-AQGR | 20 (40 μL) | 200 μL |
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| ATG2B-SLC22A17-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC22A17 Gene Summary
The Solute Carrier Family 22 Member 17 (SLC22A17) gene is located on chr14 :23815538-23822080 at 14q11.2.
Gene Name: Solute Carrier Family 22 Member 17
Chromosome: CHR14: 23815538 -23822080
Locus: 14q11.2
ATG2B Gene Summary
This gene encodes a protein required for autophagy. The encoded protein is involved in autophagosome formation. A germline duplication of a region that includes this gene is associated with predisposition to myeloid malignancies. [provided by RefSeq, Jul 2016]
Gene Name: Autophagy Related 2B
Chromosome: CHR14: 96747594 -96829678
Locus: 14q32.2
Gene Diseases
The ATG2B SLC22A17 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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