SNX9-ZDHHC14 Fusion FISH Probe
The SNX9-ZDHHC14 Fusion FISH Probe is used to confirm a fusion of the SNX9 and ZDHHC14 genes. The fusion of the SNX9 and ZDHHC14 genes has been associated with Uterine Corpus Endometrial Carcinoma, and Stomach 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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| SNX9-ZDHHC14-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-RERE | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-REOR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-REGO | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-REGR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-REAQ | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-ORRE | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-OROR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-ORGO | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GORE | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GOOR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GOGO | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GROR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GRGR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-AQRE | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-AQGO | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-AQGR | 20 (40 μL) | 200 μL |
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| SNX9-ZDHHC14-20-AQAQ | 20 (40 μL) | 200 μL |
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SNX9 Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phosphoinositide binding domain, and are involved in intracellular trafficking. The encoded protein does not contain a coiled coil region, like some family members, but does contain a SRC homology domain near its N-terminus. The encoded protein is reported to have a variety of interaction partners, including of adaptor protein 2 , dynamin, tyrosine kinase non-receptor 2, Wiskott-Aldrich syndrome-like, and ARP3 actin-related protein 3. The encoded protein is implicated in several stages of intracellular trafficking, including endocytosis, macropinocytosis, and F-actin nucleation. [provided by RefSeq, Jul 2013]
Gene Name: Sorting Nexin 9
Chromosome: CHR6: 158244293 -158366109
Locus: 6q25.3
ZDHHC14 Gene Summary
The Zinc Finger DHHC-type Containing 14 (ZDHHC14) gene is located on chr6 :157802556-158094977 at 6q25.3.
Gene Name: Zinc Finger DHHC-type Containing 14
Chromosome: CHR6: 157802556 -158094977
Locus: 6q25.3
Gene Diseases
The SNX9 ZDHHC14 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Corpus Endometrial Carcinoma |
| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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