TRAPPC9-SLC30A8 Fusion FISH Probe
The TRAPPC9-SLC30A8 Fusion FISH Probe is used to confirm a fusion of the TRAPPC9 and SLC30A8 genes. The fusion of the TRAPPC9 and SLC30A8 genes has been associated with Head And Neck Squamous Cell 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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| TRAPPC9-SLC30A8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-RERE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REOR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-REAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-ORRE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-OROR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-ORGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-ORAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GORE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOOR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GOAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRRE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GROR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-GRAQ | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQRE | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQOR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQGO | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQGR | 20 (40 μL) | 200 μL |
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| TRAPPC9-SLC30A8-20-AQAQ | 20 (40 μL) | 200 μL |
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TRAPPC9 Gene Summary
This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive cognitive disability. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010]
Gene Name: Trafficking Protein Particle Complex 9
Chromosome: CHR8: 140742585 -141468678
Locus: 8q24.3
SLC30A8 Gene Summary
The protein encoded by this gene is a zinc efflux transporter involved in the accumulation of zinc in intracellular vesicles. This gene is expressed at a high level only in the pancreas, particularly in islets of Langerhans. The encoded protein colocalizes with insulin in the secretory pathway granules of the insulin-secreting INS-1 cells. Allelic variants of this gene exist that confer susceptibility to diabetes mellitus, noninsulin-dependent (NIDDM). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]
Gene Name: Solute Carrier Family 30 Member 8
Chromosome: CHR8: 117962511 -118188953
Locus: 8q24.11
Gene Diseases
The TRAPPC9 SLC30A8 Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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