GBAS-PSPH Fusion FISH Probe
The GBAS-PSPH Fusion FISH Probe is used to confirm a fusion of the GBAS and PSPH genes. The fusion of the GBAS and PSPH genes has been associated with Lung Squamous Cell 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 |
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| GBAS-PSPH-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-RERE | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-REOR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-REGO | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-REGR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-REAQ | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-ORRE | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-OROR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-ORGO | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-ORAQ | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GORE | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GOOR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GOGO | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GOGR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GOAQ | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GRRE | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GROR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GRGO | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GRGR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-GRAQ | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-AQRE | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-AQOR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-AQGO | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-AQGR | 20 (40 μL) | 200 μL |
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| GBAS-PSPH-20-AQAQ | 20 (40 μL) | 200 μL |
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PSPH Gene Summary
The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008]
Gene Name: Phosphoserine Phosphatase
Chromosome: CHR7: 56078743 -56119268
Locus: 7p11.2
Gene Diseases
The GBAS PSPH Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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