SPTA1-GRIP1 Fusion FISH Probe
The SPTA1-GRIP1 Fusion FISH Probe is used to confirm a fusion of the SPTA1 and GRIP1 genes. The fusion of the SPTA1 and GRIP1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| SPTA1-GRIP1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-RERE | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-REOR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-REGO | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-REGR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-REAQ | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-ORRE | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-OROR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-ORGO | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GORE | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GOOR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GOGO | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GOGR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GRRE | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GROR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GRGO | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GRGR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-AQRE | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-AQOR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-AQGO | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-AQGR | 20 (40 μL) | 200 μL |
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| SPTA1-GRIP1-20-AQAQ | 20 (40 μL) | 200 μL |
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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
GRIP1 Gene Summary
This gene encodes a member of the glutamate receptor interacting protein family. The encoded scaffold protein binds to and mediates the trafficking and membrane organization of a number of transmembrane proteins. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, May 2010]
Gene Name: Glutamate Receptor Interacting Protein 1
Chromosome: CHR12: 66741210 -67072925
Locus: 12q14.3
Gene Diseases
The SPTA1 GRIP1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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