Gene-specific Copy Number Variation Probe-NSMCE2
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Catalog: |
CNVFP-NSMCE2-14361 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NSMCE2). 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: |
NSMCE2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NSMCE2 genes. This product achieves the purpose of detection by hybridizing with the NSMCE2 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 |
NSE2/MMS21 Homolog, SMC5-SMC6 Complex SUMO Ligase |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of a family of E3 small ubiquitin-related modifier (SUMO) ligases that mediates the attachment of a SUMO protein to proteins involved in nuclear transport, transcription, chromosome segregation and DNA repair. The encoded protein is part of the structural maintenance of chromosomes (SMC) 5/6 complex which plays a key role genome maintenance, facilitating chromosome segregation and suppressing mitotic recombination. A knockout of the orthologous mouse gene is lethal prior to embryonic day 10.5. Naturally occurring mutations in this gene, that abolish the SUMO ligase activity, are associated with primordial dwarfism and extreme insulin resistance. [provided by RefSeq, Mar 2017] |
Gene Symbol |
NSMCE2 |
Location |
8q24.13 |
Chromosome |
Chromosome8 |
Coordinates |
This gene maps to 126104082-126379367 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-NSMCE2-14361-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-NSMCE2-14361-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-NSMCE2-14361-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-NSMCE2-14361-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-NSMCE2-14361-AQ |
467nm |
418nm |
|
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