AGAP1-ADAMTS2 Fusion FISH Probe
The AGAP1-ADAMTS2 Fusion FISH Probe is used to confirm a fusion of the AGAP1 and ADAMTS2 genes. The fusion of the AGAP1 and ADAMTS2 genes has been associated with Prostate Adenocarcinoma. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| AGAP1-ADAMTS2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-RERE | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-REOR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-REGO | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-REGR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-OROR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GORE | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GROR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| AGAP1-ADAMTS2-20-AQAQ | 20 (40 μL) | 200 μL |
|
ADAMTS2 Gene Summary
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016]
Gene Name: ADAM Metallopeptidase With Thrombospondin Type 1 Motif 2
Chromosome: CHR5: 178537851 -178772431
Locus: 5q35.3
AGAP1 Gene Summary
This gene encodes a member of an ADP-ribosylation factor GTPase-activating protein family involved in membrane trafficking and cytoskeleton dynamics. This gene functions as a direct regulator of the adaptor-related protein complex 3 on endosomes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Gene Name: ArfGAP With GTPase Domain, Ankyrin Repeat And PH Domain 1
Chromosome: CHR2: 236402735 -237034120
Locus: 2q37.2
Gene Diseases
The AGAP1 ADAMTS2 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|