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Gene-specific Break Apart Probe-BBS2

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Catalog: GBAFP-BBS2-00670
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (BBS2). 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: BBS2 Gene-specific Break Apart Probe is designed to detect potential BBS2 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 Bardet-Biedl Syndrome 2
Gene Summary [Provided by RefSeq] This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.[provided by RefSeq, Oct 2014]
Gene Symbol BBS2
Location 16q13
Chromosome Chromosome16
Coordinates This gene maps to 56518258-56554008 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 GR; OR GBAFP-BBS2-00670-GROR 515nm;573nm 491nm;548nm
2 AQ; OR GBAFP-BBS2-00670-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-BBS2-00670-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-BBS2-00670-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-BBS2-00670-GRGO 515nm;551nm 491nm;525nm
6 GR; RE GBAFP-BBS2-00670-GRRE 515nm;599nm 491nm;580nm
7 OR; GR GBAFP-BBS2-00670-ORGR 573nm;515nm 548nm;491nm
8 RE; GO GBAFP-BBS2-00670-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-BBS2-00670-REGR 599nm;515nm 580nm;491nm

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