PEX3-SLC35F1 Fusion FISH Probe
The PEX3-SLC35F1 Fusion FISH Probe is used to confirm a fusion of the PEX3 and SLC35F1 genes. The fusion of the PEX3 and SLC35F1 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 |
|---|---|---|---|---|
| PEX3-SLC35F1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-RERE | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-REOR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-REGO | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-REGR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-OROR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GORE | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GROR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| PEX3-SLC35F1-20-AQAQ | 20 (40 μL) | 200 μL |
|
PEX3 Gene Summary
The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
Gene Name: Peroxisomal Biogenesis Factor 3
Chromosome: CHR6: 143771917 -143811751
Locus: 6q24.2
SLC35F1 Gene Summary
The Solute Carrier Family 35 Member F1 (SLC35F1) gene is located on chr6 :118228688-118638839 at 6q22.2-q22.31.
Gene Name: Solute Carrier Family 35 Member F1
Chromosome: CHR6: 118228688 -118638839
Locus: 6q22.2-q22.31
Gene Diseases
The PEX3 SLC35F1 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|