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Gene-specific Break Apart Probe-BRWD1

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Catalog: GBAFP-BRWD1-00706
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (BRWD1). 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: BRWD1 Gene-specific Break Apart Probe is designed to detect potential BRWD1 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 Bromodomain And WD Repeat Domain Containing 1
Gene Summary [Provided by RefSeq] This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) residues which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 2 bromodomains and multiple WD repeats. This gene is located within the Down syndrome region-2 on chromosome 21. Alternative splicing of this gene generates multiple transcript variants encoding distinct isoforms. In mouse, this gene encodes a nuclear protein that has a polyglutamine-containing region that functions as a transcriptional activation domain which may regulate chromatin remodelling and associates with a component of the SWI/SNF chromatin remodelling complex.[provided by RefSeq, Jun 2011]
Gene Symbol BRWD1
Location 21q22.2
Chromosome Chromosome21
Coordinates This gene maps to 40557403-40685712 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 GR; OR GBAFP-BRWD1-00706-GROR 515nm;573nm 491nm;548nm
2 AQ; OR GBAFP-BRWD1-00706-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-BRWD1-00706-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-BRWD1-00706-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-BRWD1-00706-GRGO 515nm;551nm 491nm;525nm
6 GR; RE GBAFP-BRWD1-00706-GRRE 515nm;599nm 491nm;580nm
7 OR; GR GBAFP-BRWD1-00706-ORGR 573nm;515nm 548nm;491nm
8 RE; GO GBAFP-BRWD1-00706-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-BRWD1-00706-REGR 599nm;515nm 580nm;491nm

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