KHDC1-SLC17A5 Fusion FISH Probe
The KHDC1-SLC17A5 Fusion FISH Probe is used to confirm a fusion of the KHDC1 and SLC17A5 genes. The fusion of the KHDC1 and SLC17A5 genes has been associated with Esophageal 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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| KHDC1-SLC17A5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-RERE | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-REOR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-REGO | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-REGR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-REAQ | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-ORRE | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-OROR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-ORGO | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-ORAQ | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GORE | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GOOR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GOGO | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GOGR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GOAQ | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GRRE | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GROR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GRGO | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GRGR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-GRAQ | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-AQRE | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-AQOR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-AQGO | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-AQGR | 20 (40 μL) | 200 μL |
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| KHDC1-SLC17A5-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC17A5 Gene Summary
This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]
Gene Name: Solute Carrier Family 17 Member 5
Chromosome: CHR6: 74303101 -74363737
Locus: 6q13
KHDC1 Gene Summary
The KH Domain Containing 1 (KHDC1) gene is located on chr6 :73951037-73972907 at 6q13.
Gene Name: KH Domain Containing 1
Chromosome: CHR6: 73951037 -73972907
Locus: 6q13
Gene Diseases
The KHDC1 SLC17A5 Fusion has been associated with the following diseases:
| Disease Name |
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| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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