MFN2 Break Apart FISH Probe
Empire Genomics’ MFN2 Break Apart FISH Probe is designed to flank the MFN2 gene and is typically used for detecting MFN2 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** 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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MFN2BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
MFN2BA-20-AQOR | 20 (40 μL) | 200 μL | ||
MFN2BA-20-GOGR | 20 (40 μL) | 200 μL | ||
MFN2BA-20-GORE | 20 (40 μL) | 200 μL | ||
MFN2BA-20-GRGO | 20 (40 μL) | 200 μL | ||
MFN2BA-20-GROR | 20 (40 μL) | 200 μL | ||
MFN2BA-20-GRRE | 20 (40 μL) | 200 μL | ||
MFN2BA-20-REGO | 20 (40 μL) | 200 μL | ||
MFN2BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: MFN2
Gene Name: Mitofusin 2
Chromosome: CHR1: 12040237-12073572
Locus: 1p36.22
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: MFN2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: MFN2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping