Gene-specific Copy Number Variation Probe-SNX15
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Catalog: |
CNVFP-SNX15-19521 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNX15). 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: |
SNX15 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNX15 genes. This product achieves the purpose of detection by hybridizing with the SNX15 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 |
Sorting Nexin 15 |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010] |
Gene Symbol |
SNX15 |
Location |
11q13.1 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 64794879-64808044 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-SNX15-19521-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SNX15-19521-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SNX15-19521-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SNX15-19521-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SNX15-19521-AQ |
467nm |
418nm |
|
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