SNX29-HS3ST4 Fusion FISH Probe
The SNX29-HS3ST4 Fusion FISH Probe is used to confirm a fusion of the SNX29 and HS3ST4 genes. The fusion of the SNX29 and HS3ST4 genes has been associated with Skin Cutaneous Melanoma. 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-HS3ST4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-RERE | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-REOR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-REGO | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-REGR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-REAQ | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-ORRE | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-OROR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-ORGO | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-ORAQ | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GORE | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GOOR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GOGO | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GOGR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GOAQ | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GRRE | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GROR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GRGO | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GRGR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-GRAQ | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-AQRE | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-AQOR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-AQGO | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-AQGR | 20 (40 μL) | 200 μL | ||
SNX29-HS3ST4-20-AQAQ | 20 (40 μL) | 200 μL |
HS3ST4 Gene Summary
This gene encodes the enzyme heparan sulfate D-glucosaminyl 3-O-sulfotransferase 4. This enzyme generates 3-O-sulfated glucosaminyl residues in heparan sulfate. Cell surface heparan sulfate is used as a receptor by herpes simplex virus type 1 (HSV-1), and expression of this gene is thought to play a role in HSV-1 pathogenesis. [provided by RefSeq, Jul 2008]
Gene Name: Heparan Sulfate-glucosamine 3-sulfotransferase 4
Chromosome: CHR16: 25703346 -26149009
Locus: 16p12.1
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 HS3ST4 Fusion has been associated with the following diseases:
Disease Name |
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Skin Cutaneous Melanoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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