Gene-specific Copy Number Variation Probe-SECISBP2
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| Catalog: |
CNVFP-SECISBP2-18316 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SECISBP2). 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: |
SECISBP2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SECISBP2 genes. This product achieves the purpose of detection by hybridizing with the SECISBP2 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 |
SECIS Binding Protein 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is one of the essential components of the machinery involved in co-translational insertion of selenocysteine (Sec) into selenoproteins. Sec is encoded by the UGA codon, which normally signals translation termination. The recoding of UGA as Sec codon requires a Sec insertion sequence (SECIS) element; present in the 3' untranslated regions of eukaryotic selenoprotein mRNAs. This protein specifically binds to the SECIS element, which is stimulated by a Sec-specific translation elongation factor. Mutations in this gene have been associated with reduction in enzymatic activity of type II iodothyronine deiodinase (a selenoprotein) and abnormal thyroid hormone metabolism. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
SECISBP2 |
| Location |
9q22.2 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 91933411-91974561 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-SECISBP2-18316-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SECISBP2-18316-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SECISBP2-18316-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SECISBP2-18316-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SECISBP2-18316-AQ |
467nm |
418nm |
|
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