Gene-specific Copy Number Variation Probe-PSTPIP1
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| Catalog: |
CNVFP-PSTPIP1-16746 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PSTPIP1). 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: |
PSTPIP1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PSTPIP1 genes. This product achieves the purpose of detection by hybridizing with the PSTPIP1 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 |
Proline-serine-threonine Phosphatase Interacting Protein 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a cytoskeletal protein that is highly expressed in hemopoietic tissues. This protein functions via its interaction with several different proteins involved in cytoskeletal organization and inflammatory processes. It binds to the cytoplasmic tail of CD2, an effector of T cell activation and adhesion, downregulating CD2-triggered adhesion. It binds PEST-type protein tyrosine phosphatases (PTP) and directs them to c-Abl kinase to mediate c-Abl dephosphorylation, thereby, regulating c-Abl activity. It also interacts with pyrin, which is found in association with the cytoskeleton in myeloid/monocytic cells and modulates immunoregulatory functions. Mutations in this gene are associated with PAPA (pyogenic sterile arthritis, pyoderma gangrenosum, and acne) syndrome. It is hypothesized that the disease-causing mutations compromise physiologic signaling necessary for the maintenance of a proper inflammatory response. [provided by RefSeq, Mar 2016] |
| Gene Symbol |
PSTPIP1 |
| Location |
15q24.3 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 77287464-77329671 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-PSTPIP1-16746-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PSTPIP1-16746-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PSTPIP1-16746-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PSTPIP1-16746-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PSTPIP1-16746-AQ |
467nm |
418nm |
|
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