Gene-specific Copy Number Variation Probe-SPN
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| Catalog: |
CNVFP-SPN-19638 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPN). 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: |
SPN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPN genes. This product achieves the purpose of detection by hybridizing with the SPN 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 |
Sialophorin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a highly sialylated glycoprotein that functions in antigen-specific activation of T cells, and is found on the surface of thymocytes, T lymphocytes, monocytes, granulocytes, and some B lymphocytes. It contains a mucin-like extracellular domain, a transmembrane region and a carboxy-terminal intracellular region. The extracellular domain has a high proportion of serine and threonine residues, allowing extensive O-glycosylation, and has one potential N-glycosylation site, while the carboxy-terminal region has potential phosphorylation sites that may mediate transduction of activation signals. Different glycoforms of this protein have been described. In stimulated immune cells, proteolytic cleavage of the extracellular domain occurs in some cell types, releasing a soluble extracellular fragment. Defects in expression of this gene are associated with Wiskott-Aldrich syndrome. [provided by RefSeq, Sep 2017] |
| Gene Symbol |
SPN |
| Location |
16p11.2 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 29674299-29681823 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-SPN-19638-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SPN-19638-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SPN-19638-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SPN-19638-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SPN-19638-AQ |
467nm |
418nm |
|
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