GNS-SLC16A7 Fusion FISH Probe
The GNS-SLC16A7 Fusion FISH Probe is used to confirm a fusion of the GNS and SLC16A7 genes. The fusion of the GNS and SLC16A7 genes has been associated with Sarcoma. 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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| GNS-SLC16A7-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-RERE | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-REOR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-REGO | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-REGR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-REAQ | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-ORRE | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-OROR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-ORGO | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-ORAQ | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GORE | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GOOR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GOGO | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GOGR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GOAQ | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GRRE | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GROR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GRGO | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GRGR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-GRAQ | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-AQRE | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-AQOR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-AQGO | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-AQGR | 20 (40 μL) | 200 μL |
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| GNS-SLC16A7-20-AQAQ | 20 (40 μL) | 200 μL |
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GNS Gene Summary
The product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome. [provided by RefSeq, Jul 2008]
Gene Name: Glucosamine (N-acetyl)-6-sulfatase
Chromosome: CHR12: 65107221 -65153226
Locus: 12q14.3
SLC16A7 Gene Summary
This gene is a member of the monocarboxylate transporter family. Members in this family transport metabolites, such as lactate, pyruvate, and ketone bodies. The protein encoded by this gene catalyzes the proton-linked transport of monocarboxylates and has the highest affinity for pyruvate. This protein has been reported to be more highly expressed in prostate and colorectal cancer specimens when compared to control specimens. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]
Gene Name: Solute Carrier Family 16 Member 7
Chromosome: CHR12: 60083125 -60175408
Locus: 12q14.1
Gene Diseases
The GNS SLC16A7 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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