MNX1 FISH Probe
Empire Genomics has developed a MNX1 FISH probe to detect MNX1 gene aneusomy. The MNX1 FISH probe comes labeled in orange, and you may also choose to customize the probe to meet your needs.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
Turnaround Time: 7-10 Business Days Shipping Time: 1-2 Day Expedited Shipping
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| MNX1-20-OR (Standard Design) | 20 (40 μL) | 200 μL |
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| MNX1-20-GO | 20 (40 μL) | 200 μL |
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| MNX1-20-GR | 20 (40 μL) | 200 μL |
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| MNX1-20-AQ | 20 (40 μL) | 200 μL |
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| MNX1-20-RE | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Gene Details
Gene Symbol: MNX1
Gene Name: Motor Neuron And Pancreas Homeobox 1
Chromosome: CHR7: 156797546-156803347
Locus: 7q36.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
There are currently no FISH related publications for this gene.