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| Catalog: | GBAFP-PSTPIP1-16305 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PSTPIP1). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent. |
| Application: | PSTPIP1 Gene-specific Break Apart Probe is designed to detect potential PSTPIP1 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services. |
| Quantity: | 20 Tests |
| Probe Kits Volume (µL): | 40 μL |
| Hybridization Solution (µL): | 200 μL |
| Turnaround Time: | Within 10 Business Days |
| Shipping Time: | 1-2 Day Expedited Shipping |
| Shipping Conditions: | -20℃ |
| Storage Conditions: | Store at -20℃ and avoid light; |
| 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 |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-PSTPIP1-16305-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-PSTPIP1-16305-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PSTPIP1-16305-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PSTPIP1-16305-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PSTPIP1-16305-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-PSTPIP1-16305-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-PSTPIP1-16305-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-PSTPIP1-16305-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PSTPIP1-16305-REGR | 599nm;515nm | 580nm;491nm |
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