Gene-specific Copy Number Variation Probe-STAP1
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| Catalog: |
CNVFP-STAP1-20135 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (STAP1). 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: |
STAP1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to STAP1 genes. This product achieves the purpose of detection by hybridizing with the STAP1 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 |
Signal Transducing Adaptor Family Member 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene contains a proline-rich region, a pleckstrin homology (PH) domain, and a region in the carboxy terminal half with similarity to the Src Homology 2 (SH2) domain. This protein is a substrate of tyrosine-protein kinase Tec, and its interaction with tyrosine-protein kinase Tec is phosphorylation-dependent. This protein is thought to participate in a positive feedback loop by upregulating the activity of tyrosine-protein kinase Tec. Variants of this gene have been associated with autosomal-dominant hypercholesterolemia (ADH), which is characterized by elevated low-density lipoprotein cholesterol levels and in increased risk of coronary vascular disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
| Gene Symbol |
STAP1 |
| Location |
4q13.2 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 68424445-68472616 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-STAP1-20135-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-STAP1-20135-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-STAP1-20135-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-STAP1-20135-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-STAP1-20135-AQ |
467nm |
418nm |
|
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