Gene-specific Copy Number Variation Probe-MFN2
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Catalog: |
CNVFP-MFN2-11206 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MFN2). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
Application: |
MFN2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MFN2 genes. This product achieves the purpose of detection by hybridizing with the MFN2 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
Category: |
Copy Number Variation |
Probe Kits Volume (µL): |
40 μL |
Quantity: |
20 Tests |
Hybridization Solution (µL): |
200 μL |
Turnaround Time: |
7-10 Business Days |
Shipping Time: |
1-2 Day Expedited Shipping |
Storage Conditions: |
Store at -20℃ and avoid light; |
Shipping Conditions: |
-20℃ |
Gene Details
Gene Name |
Mitofusin 2 |
Gene Summary [Provided by RefSeq] |
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 Symbol |
MFN2 |
Location |
1p36.22 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 12040237-12073572 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
1 |
OR
|
CNVFP-MFN2-11206-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-MFN2-11206-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-MFN2-11206-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-MFN2-11206-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-MFN2-11206-AQ |
467nm |
418nm |
|
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