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Gene-specific Break Apart Probe-TYROBP

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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 Details

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

Order Sheet

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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