Gene-specific Copy Number Variation Probe-SEPHS2
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Catalog: |
CNVFP-SEPHS2-18244 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SEPHS2). 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: |
SEPHS2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SEPHS2 genes. This product achieves the purpose of detection by hybridizing with the SEPHS2 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 |
Selenophosphate Synthetase 2 |
Gene Summary [Provided by RefSeq] |
This gene encodes an enzyme that catalyzes the production of monoselenophosphate (MSP) from selenide and ATP. MSP is the selenium donor required for synthesis of selenocysteine (Sec), which is co-translationally incorporated into selenoproteins at in-frame UGA codons that normally signal translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein is itself a selenoprotein containing a Sec residue at its active site, suggesting the existence of an autoregulatory mechanism. It is preferentially expressed in tissues implicated in the synthesis of selenoproteins and in sites of blood cell development. A pseudogene for this locus has been identified on chromosome 5. [provided by RefSeq, May 2017] |
Gene Symbol |
SEPHS2 |
Location |
16p11.2 |
Chromosome |
Chromosome16 |
Coordinates |
This gene maps to 30454951-30457224 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-SEPHS2-18244-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SEPHS2-18244-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SEPHS2-18244-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SEPHS2-18244-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SEPHS2-18244-AQ |
467nm |
418nm |
|
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