EFEMP2-C6ORF132 Fusion FISH Probe
The EFEMP2-C6ORF132 Fusion FISH Probe is used to confirm a fusion of the EFEMP2 and C6ORF132 genes. The fusion of the EFEMP2 and C6ORF132 genes has been associated with Stomach 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 |
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| EFEMP2-C6ORF132-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-RERE | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-REOR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-REGO | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-REGR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-REAQ | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-ORRE | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-OROR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-ORGO | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-ORAQ | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GORE | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GOOR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GOGO | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GOGR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GOAQ | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GRRE | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GROR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GRGO | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GRGR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-GRAQ | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-AQRE | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-AQOR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-AQGO | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-AQGR | 20 (40 μL) | 200 μL |
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| EFEMP2-C6ORF132-20-AQAQ | 20 (40 μL) | 200 μL |
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EFEMP2 Gene Summary
A large number of extracellular matrix proteins have been found to contain variations of the epidermal growth factor (EGF) domain and have been implicated in functions as diverse as blood coagulation, activation of complement and determination of cell fate during development. The protein encoded by this gene contains four EGF2 domains and six calcium-binding EGF2 domains. This gene is necessary for elastic fiber formation and connective tissue development. Defects in this gene are cause of an autosomal recessive cutis laxa syndrome. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jan 2011]
Gene Name: EGF Containing Fibulin Extracellular Matrix Protein 2
Chromosome: CHR11: 65633911 -65640405
Locus: 11q13.1
C6orf132 Gene Summary
The Chromosome 6 Open Reading Frame 132 (C6orf132) gene is located on chr6 :42068856-42110715 at 6p21.1.
Gene Name: Chromosome 6 Open Reading Frame 132
Chromosome: CHR6: 42068856 -42110715
Locus: 6p21.1
Gene Diseases
The EFEMP2 C6ORF132 Fusion has been associated with the following diseases:
| Disease Name |
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| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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