ERBB2IP-ASXL1 Fusion FISH Probe
The ERBB2IP-ASXL1 Fusion FISH Probe is used to confirm a fusion of the ERBB2IP and ASXL1 genes. The fusion of the ERBB2IP and ASXL1 genes has been associated with Lung 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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| ERBB2IP-ASXL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-RERE | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-REOR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-REGO | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-REGR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-REAQ | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-ORRE | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-OROR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-ORGO | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-ORAQ | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GORE | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GOOR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GOGO | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GOGR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GOAQ | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GRRE | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GROR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GRGO | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GRGR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-GRAQ | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-AQRE | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-AQOR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-AQGO | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-AQGR | 20 (40 μL) | 200 μL |
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| ERBB2IP-ASXL1-20-AQAQ | 20 (40 μL) | 200 μL |
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ASXL1 Gene Summary
This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Gene Name: Additional Sex Combs Like 1, Transcriptional Regulator
Chromosome: CHR20: 30946146 -31027122
Locus: 20q11.21
Gene Diseases
The ERBB2IP ASXL1 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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