Gene-specific Copy Number Variation Probe-SOX2
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| Catalog: |
CNVFP-SOX2-19765 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SOX2). 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: |
SOX2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SOX2 genes. This product achieves the purpose of detection by hybridizing with the SOX2 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 |
SRY-box 2 |
| Gene Summary [Provided by RefSeq] |
This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008] |
| Gene Symbol |
SOX2 |
| Location |
3q26.33 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 181429711-181432223 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-SOX2-19765-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SOX2-19765-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SOX2-19765-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SOX2-19765-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SOX2-19765-AQ |
467nm |
418nm |
|
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