Gene-specific Copy Number Variation Probe-SNAPIN
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Catalog: |
CNVFP-SNAPIN-18896 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNAPIN). 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: |
SNAPIN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNAPIN genes. This product achieves the purpose of detection by hybridizing with the SNAPIN 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 |
SNAP Associated Protein |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a coiled-coil-forming protein that associates with the SNARE (soluble N-ethylmaleimide-sensitive fusion protein attachment protein receptor) complex of proteins and the BLOC-1 (biogenesis of lysosome-related organelles) complex. Biochemical studies have identified additional binding partners. As part of the SNARE complex, it is required for vesicle docking and fusion and regulates neurotransmitter release. The BLOC-1 complex is required for the biogenesis of specialized organelles such as melanosomes and platelet dense granules. Mutations in gene products that form the BLOC-1 complex have been identified in mouse strains that are models of Hermansky-Pudlak syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012] |
Gene Symbol |
SNAPIN |
Location |
1q21.3 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 153631144-153634326 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-SNAPIN-18896-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SNAPIN-18896-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SNAPIN-18896-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SNAPIN-18896-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SNAPIN-18896-AQ |
467nm |
418nm |
|
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