SLC39A9-SEC23IP Fusion FISH Probe
The SLC39A9-SEC23IP Fusion FISH Probe is used to confirm a fusion of the SLC39A9 and SEC23IP genes. The fusion of the SLC39A9 and SEC23IP genes has been associated with Ovarian Serous Cystadenocarcinoma. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| SLC39A9-SEC23IP-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-RERE | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-REOR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-REGO | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-REGR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-OROR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GORE | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GROR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC39A9-SEC23IP-20-AQAQ | 20 (40 μL) | 200 μL |
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SEC23IP Gene Summary
This gene encodes a member of the phosphatidic acid preferring-phospholipase A1 family. The encoded protein is localized to endoplasmic reticulum exit sites and plays a critical role in ER-Golgi transport as part of the multimeric coat protein II complex. An orthologous gene in frogs is required for normal neural crest cell development, suggesting that this gene may play a role in Waardenburg syndrome neural crest defects. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]
Gene Name: SEC23 Interacting Protein
Chromosome: CHR10: 121652084 -121704170
Locus: 10q26.11-q26.12
SLC39A9 Gene Summary
The Solute Carrier Family 39 Member 9 (SLC39A9) gene is located on chr14 :69865406-69929107 at 14q24.1.
Gene Name: Solute Carrier Family 39 Member 9
Chromosome: CHR14: 69865406 -69929107
Locus: 14q24.1
Gene Diseases
The SLC39A9 SEC23IP Fusion has been associated with the following diseases:
| Disease Name |
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| Ovarian Serous Cystadenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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