Gene-specific Copy Number Variation Probe-MAGED2
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Catalog: |
CNVFP-MAGED2-10916 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MAGED2). 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: |
MAGED2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MAGED2 genes. This product achieves the purpose of detection by hybridizing with the MAGED2 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 |
MAGE Family Member D2 |
Gene Summary [Provided by RefSeq] |
This gene is a member of the MAGED gene family. The MAGED genes are clustered on chromosome Xp11. This gene is located in Xp11.2, a hot spot for X-linked intellectual disability (XLID). Mutations in this gene cause a form of transient antenatal Bartter's syndrome. This gene may also be involved in several types of cancer, including breast cancer and melanoma. The protein encoded by this gene is progressively recruited from the cytoplasm to the nucleoplasm during the interphase and after nucleolar stress and is thus thought to play a role in cell cycle regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017] |
Gene Symbol |
MAGED2 |
Location |
Xp11.21 |
Chromosome |
ChromosomeX |
Coordinates |
This gene maps to 54834170-54842445 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-MAGED2-10916-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-MAGED2-10916-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-MAGED2-10916-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-MAGED2-10916-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-MAGED2-10916-AQ |
467nm |
418nm |
|
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