Gene-specific Copy Number Variation Probe-SNX9
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Catalog: |
CNVFP-SNX9-19478 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNX9). 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: |
SNX9 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNX9 genes. This product achieves the purpose of detection by hybridizing with the SNX9 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 9 |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the sorting nexin family. Members of this family contain a phosphoinositide binding domain, and are involved in intracellular trafficking. The encoded protein does not contain a coiled coil region, like some family members, but does contain a SRC homology domain near its N-terminus. The encoded protein is reported to have a variety of interaction partners, including of adaptor protein 2 , dynamin, tyrosine kinase non-receptor 2, Wiskott-Aldrich syndrome-like, and ARP3 actin-related protein 3. The encoded protein is implicated in several stages of intracellular trafficking, including endocytosis, macropinocytosis, and F-actin nucleation. [provided by RefSeq, Jul 2013] |
Gene Symbol |
SNX9 |
Location |
6q25.3 |
Chromosome |
Chromosome6 |
Coordinates |
This gene maps to 158244293-158366109 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-SNX9-19478-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SNX9-19478-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SNX9-19478-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SNX9-19478-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SNX9-19478-AQ |
467nm |
418nm |
|
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