ST7-CNTNAP2 Fusion FISH Probe
The ST7-CNTNAP2 Fusion FISH Probe is used to confirm a fusion of the ST7 and CNTNAP2 genes. The fusion of the ST7 and CNTNAP2 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 |
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| ST7-CNTNAP2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-RERE | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-REOR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-REGO | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-REGR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-REAQ | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-ORRE | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-OROR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-ORGO | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-ORAQ | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GORE | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GOOR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GOGO | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GOGR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GOAQ | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GRRE | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GROR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GRGO | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GRGR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-GRAQ | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-AQRE | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-AQOR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-AQGO | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-AQGR | 20 (40 μL) | 200 μL |
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| ST7-CNTNAP2-20-AQAQ | 20 (40 μL) | 200 μL |
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ST7 Gene Summary
The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]
Gene Name: Suppression Of Tumorigenicity 7
Chromosome: CHR7: 116593380 -116870075
Locus: 7q31.2
CNTNAP2 Gene Summary
This gene encodes a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons, and mediates interactions between neurons and glia during nervous system development and is also involved in localization of potassium channels within differentiating axons. This gene encompasses almost 1.5% of chromosome 7 and is one of the largest genes in the human genome. It is directly bound and regulated by forkhead box protein P2, a transcription factor related to speech and language development. This gene has been implicated in multiple neurodevelopmental disorders, including Gilles de la Tourette syndrome, schizophrenia, epilepsy, autism, ADHD and intellectual disability. [provided by RefSeq, Jul 2017]
Gene Name: Contactin Associated Protein Like 2
Chromosome: CHR7: 145813452 -148118088
Locus: 7q35-q36.1
Gene Diseases
The ST7 CNTNAP2 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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