PUM1-HS2ST1 Fusion FISH Probe
The PUM1-HS2ST1 Fusion FISH Probe is used to confirm a fusion of the PUM1 and HS2ST1 genes. The fusion of the PUM1 and HS2ST1 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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| PUM1-HS2ST1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-RERE | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-REOR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-REGO | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-REGR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-REAQ | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-ORRE | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-OROR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-ORGO | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-ORAQ | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GORE | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GOOR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GOGO | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GOGR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GOAQ | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GRRE | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GROR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GRGO | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GRGR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-GRAQ | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-AQRE | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-AQOR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-AQGO | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-AQGR | 20 (40 μL) | 200 μL |
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| PUM1-HS2ST1-20-AQAQ | 20 (40 μL) | 200 μL |
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HS2ST1 Gene Summary
Heparan sulfate biosynthetic enzymes are key components in generating a myriad of distinct heparan sulfate fine structures that carry out multiple biologic activities. This gene encodes a member of the heparan sulfate biosynthetic enzyme family that transfers sulfate to the 2 position of the iduronic acid residue of heparan sulfate. The disruption of this gene resulted in no kidney formation in knockout embryonic mice, indicating that the absence of this enzyme may interfere with the signaling required for kidney formation. Two alternatively spliced transcript variants that encode different proteins have been found for this gene. [provided by RefSeq, Aug 2008]
Gene Name: Heparan Sulfate 2-O-sulfotransferase 1
Chromosome: CHR1: 87380334 -87575681
Locus: 1p22.3
PUM1 Gene Summary
This gene encodes a member of the PUF family, evolutionarily conserved RNA-binding proteins related to the Pumilio proteins of Drosophila and the fem-3 mRNA binding factor proteins of C. elegans. The encoded protein contains a sequence-specific RNA binding domain comprised of eight repeats and N- and C-terminal flanking regions, and serves as a translational regulator of specific mRNAs by binding to their 3' untranslated regions. The evolutionarily conserved function of the encoded protein in invertebrates and lower vertebrates suggests that the human protein may be involved in translational regulation of embryogenesis, and cell development and differentiation. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Name: Pumilio RNA Binding Family Member 1
Chromosome: CHR1: 31404352 -31538564
Locus: 1p35.2
Gene Diseases
The PUM1 HS2ST1 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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