SNX29-CLEC16A Fusion FISH Probe
The SNX29-CLEC16A Fusion FISH Probe is used to confirm a fusion of the SNX29 and CLEC16A genes. The fusion of the SNX29 and CLEC16A genes has been associated with Lung Adenocarcinoma, and Uterine Corpus Endometrial 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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| SNX29-CLEC16A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-RERE | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-REOR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-REGO | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-REGR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-REAQ | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-ORRE | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-OROR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-ORGO | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GORE | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GOOR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GOGO | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GROR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GRGR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-AQRE | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-AQGO | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-AQGR | 20 (40 μL) | 200 μL |
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| SNX29-CLEC16A-20-AQAQ | 20 (40 μL) | 200 μL |
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CLEC16A Gene Summary
This gene encodes a member of the C-type lectin domain containing family. Single nucleotide polymorphisms in introns of this gene have been associated with diabetes mellitus, multiple sclerosis and rheumatoid arthritis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]
Gene Name: C-type Lectin Domain Containing 16A
Chromosome: CHR16: 11038344 -11276046
Locus: 16p13.13
SNX29 Gene Summary
The Sorting Nexin 29 (SNX29) gene is located on chr16 :12070601-12668146 at 16p13.13-p13.12.
Gene Name: Sorting Nexin 29
Chromosome: CHR16: 12070601 -12668146
Locus: 16p13.13-p13.12
Gene Diseases
The SNX29 CLEC16A Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
| Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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