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| Catalog: | GBAFP-WISP3-18841 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (WISP3). 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: | WISP3 Gene-specific Break Apart Probe is designed to detect potential WISP3 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 | WNT1 Inducible Signaling Pathway Protein 3 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like domain. This gene is overexpressed in colon tumors. It may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. Mutations of this gene are associated with progressive pseudorheumatoid dysplasia, an autosomal recessive skeletal disorder, indicating that the gene is essential for normal postnatal skeletal growth and cartilage homeostasis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol | WISP3 |
| Location | 6q21 |
| Chromosome | Chromosome6 |
| Coordinates | This gene maps to 112375277-112390887 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-WISP3-18841-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-WISP3-18841-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-WISP3-18841-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-WISP3-18841-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-WISP3-18841-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-WISP3-18841-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-WISP3-18841-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-WISP3-18841-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-WISP3-18841-REGR | 599nm;515nm | 580nm;491nm |
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