Gene-specific Copy Number Variation Probe-PTPN11
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| Catalog: |
CNVFP-PTPN11-16684 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PTPN11). 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: |
PTPN11 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PTPN11 genes. This product achieves the purpose of detection by hybridizing with the PTPN11 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 |
Protein Tyrosine Phosphatase, Non-receptor Type 11 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP contains two tandem Src homology-2 domains, which function as phospho-tyrosine binding domains and mediate the interaction of this PTP with its substrates. This PTP is widely expressed in most tissues and plays a regulatory role in various cell signaling events that are important for a diversity of cell functions, such as mitogenic activation, metabolic control, transcription regulation, and cell migration. Mutations in this gene are a cause of Noonan syndrome as well as acute myeloid leukemia. [provided by RefSeq, Aug 2016] |
| Gene Symbol |
PTPN11 |
| Location |
12q24.13 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 112856535-112947717 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-PTPN11-16684-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PTPN11-16684-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PTPN11-16684-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PTPN11-16684-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PTPN11-16684-AQ |
467nm |
418nm |
|
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