FCGR2A-SPTA1 Fusion FISH Probe
The FCGR2A-SPTA1 Fusion FISH Probe is used to confirm a fusion of the FCGR2A and SPTA1 genes. The fusion of the FCGR2A and SPTA1 genes has been associated with Breast Invasive Carcinoma. 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 |
|---|---|---|---|---|
| FCGR2A-SPTA1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-RERE | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-REOR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-REGO | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-REGR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-OROR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GORE | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GROR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| FCGR2A-SPTA1-20-AQAQ | 20 (40 μL) | 200 μL |
|
FCGR2A Gene Summary
This gene encodes one member of a family of immunoglobulin Fc receptor genes found on the surface of many immune response cells. The protein encoded by this gene is a cell surface receptor found on phagocytic cells such as macrophages and neutrophils, and is involved in the process of phagocytosis and clearing of immune complexes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2008]
Gene Name: Fc Fragment Of IgG Receptor IIa
Chromosome: CHR1: 161475204 -161489360
Locus: 1q23.3
SPTA1 Gene Summary
This gene encodes a member of a family of molecular scaffold proteins that link the plasma membrane to the actin cytoskeleton and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms a component of the erythrocyte plasma membrane. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis-2, pyropoikilocytosis, and spherocytosis, type 3. [provided by RefSeq, Aug 2017]
Gene Name: Spectrin Alpha, Erythrocytic 1
Chromosome: CHR1: 158580495 -158656506
Locus: 1q23.1
Gene Diseases
The FCGR2A SPTA1 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|