Gene-specific Copy Number Variation Probe-SNIP1
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| Catalog: |
CNVFP-SNIP1-19244 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNIP1). 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: |
SNIP1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNIP1 genes. This product achieves the purpose of detection by hybridizing with the SNIP1 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 |
Smad Nuclear Interacting Protein 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that contains a coiled-coil motif and C-terminal forkhead-associated (FHA) domain. The encoded protein functions as a transcriptional coactivator that increases c-Myc activity and inhibits transforming growth factor beta (TGF-beta) and nuclear factor kappa-B (NF-kB) signaling. The encoded protein also regulates the stability of cyclin D1 mRNA, and may play a role in cell proliferation and cancer progression. Mutations in this gene are a cause of psychomotor retardation, epilepsy, and craniofacial dysmorphism (PMRED). [provided by RefSeq, Mar 2012] |
| Gene Symbol |
SNIP1 |
| Location |
1p34.3 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 38002141-38019903 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-SNIP1-19244-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SNIP1-19244-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SNIP1-19244-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SNIP1-19244-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SNIP1-19244-AQ |
467nm |
418nm |
|
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