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Gene-specific Break Apart Probe-PSTPIP1

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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 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

Order Sheet

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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