Gene-specific Copy Number Variation Probe-NSD2
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| Catalog: |
CNVFP-NSD2-14391 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NSD2). 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: |
NSD2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NSD2 genes. This product achieves the purpose of detection by hybridizing with the NSD2 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 |
Nuclear Receptor Binding SET Domain Protein 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
NSD2 |
| Location |
4p16.3 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 1871356-1982206 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-NSD2-14391-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NSD2-14391-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NSD2-14391-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NSD2-14391-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NSD2-14391-AQ |
467nm |
418nm |
|
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