MYO1D-HNF1B Fusion FISH Probe
The MYO1D-HNF1B Fusion FISH Probe is used to confirm a fusion of the MYO1D and HNF1B genes. The fusion of the MYO1D and HNF1B genes has been associated with Cholangiocarcinoma. 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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| MYO1D-HNF1B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-RERE | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-REOR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-REGO | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-REGR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-REAQ | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-ORRE | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-OROR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-ORGO | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-ORAQ | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GORE | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GOOR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GOGO | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GOGR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GOAQ | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GRRE | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GROR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GRGO | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GRGR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-GRAQ | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-AQRE | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-AQOR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-AQGO | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-AQGR | 20 (40 μL) | 200 μL |
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| MYO1D-HNF1B-20-AQAQ | 20 (40 μL) | 200 μL |
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MYO1D Gene Summary
The Myosin ID (MYO1D) gene is located on chr17 :30819627-31203902 at 17q11.2.
Gene Name: Myosin ID
Chromosome: CHR17: 30819627 -31203902
Locus: 17q11.2
HNF1B Gene Summary
This gene encodes a member of the homeodomain-containing superfamily of transcription factors. The protein binds to DNA as either a homodimer, or a heterodimer with the related protein hepatocyte nuclear factor 1-alpha. The gene has been shown to function in nephron development, and regulates development of the embryonic pancreas. Mutations in this gene result in renal cysts and diabetes syndrome and noninsulin-dependent diabetes mellitus, and expression of this gene is altered in some types of cancer. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
Gene Name: HNF1 Homeobox B
Chromosome: CHR17: 36046433 -36105096
Locus: 17q12
Gene Diseases
The MYO1D HNF1B Fusion has been associated with the following diseases:
| Disease Name |
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| Cholangiocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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