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| Catalog: | GBAFP-TYROBP-08809 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TYROBP). 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: | TYROBP Gene-specific Break Apart Probe is designed to detect potential TYROBP 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 | TYRO Protein Tyrosine Kinase Binding Protein |
| Gene Summary [Provided by RefSeq] | This gene encodes a transmembrane signaling polypeptide which contains an immunoreceptor tyrosine-based activation motif (ITAM) in its cytoplasmic domain. The encoded protein may associate with the killer-cell inhibitory receptor (KIR) family of membrane glycoproteins and may act as an activating signal transduction element. This protein may bind zeta-chain (TCR) associated protein kinase 70kDa (ZAP-70) and spleen tyrosine kinase (SYK) and play a role in signal transduction, bone modeling, brain myelination, and inflammation. Mutations within this gene have been associated with polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), also known as Nasu-Hakola disease. Its putative receptor, triggering receptor expressed on myeloid cells 2 (TREM2), also causes PLOSL. Multiple alternative transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Mar 2010] |
| Gene Symbol | TYROBP |
| Location | 19q13.12 |
| Chromosome | Chromosome19 |
| Coordinates | This gene maps to 36395302-36399211 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-TYROBP-08809-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-TYROBP-08809-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TYROBP-08809-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TYROBP-08809-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TYROBP-08809-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-TYROBP-08809-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-TYROBP-08809-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-TYROBP-08809-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TYROBP-08809-REGR | 599nm;515nm | 580nm;491nm |
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