Gene-specific Copy Number Variation Probe-SELENOM
Add to Cart
| Catalog: |
CNVFP-SELENOM-18303 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SELENOM). 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: |
SELENOM Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SELENOM genes. This product achieves the purpose of detection by hybridizing with the SELENOM 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 |
Selenoprotein M |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to the selenoprotein M/SEP15 family. The exact function of this protein is not known. It is localized in the perinuclear region, is highly expressed in the brain, and may be involved in neurodegenerative disorders. Transgenic mice with targeted deletion of this gene exhibit increased weight gain, suggesting a role for this gene in the regulation of body weight and energy metabolism. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec). Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. [provided by RefSeq, Dec 2016] |
| Gene Symbol |
SELENOM |
| Location |
22q12.2 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 31107564-31104776 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-SELENOM-18303-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SELENOM-18303-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SELENOM-18303-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SELENOM-18303-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SELENOM-18303-AQ |
467nm |
418nm |
|
Other Products
