Gene-specific Copy Number Variation Probe-SHOX2
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| Catalog: |
CNVFP-SHOX2-18403 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SHOX2). 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: |
SHOX2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SHOX2 genes. This product achieves the purpose of detection by hybridizing with the SHOX2 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 |
Short Stature Homeobox 2 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009] |
| Gene Symbol |
SHOX2 |
| Location |
3q25.32 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 157813799-157823952 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-SHOX2-18403-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SHOX2-18403-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SHOX2-18403-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SHOX2-18403-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SHOX2-18403-AQ |
467nm |
418nm |
|
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