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Gene-specific Break Apart Probe-GNB1L

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Catalog: GBAFP-GNB1L-03005
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (GNB1L). 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: GNB1L Gene-specific Break Apart Probe is designed to detect potential GNB1L 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 G Protein Subunit Beta 1 Like
Gene Summary [Provided by RefSeq] This gene encodes a G-protein beta-subunit-like polypeptide which is 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), 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 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene. [provided by RefSeq, Jul 2008]
Gene Symbol GNB1L
Location 22q11.21
Chromosome Chromosome22
Coordinates This gene maps to 19775933-19842462 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 GR; OR GBAFP-GNB1L-03005-GROR 515nm;573nm 491nm;548nm
2 AQ; OR GBAFP-GNB1L-03005-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-GNB1L-03005-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-GNB1L-03005-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-GNB1L-03005-GRGO 515nm;551nm 491nm;525nm
6 GR; RE GBAFP-GNB1L-03005-GRRE 515nm;599nm 491nm;580nm
7 OR; GR GBAFP-GNB1L-03005-ORGR 573nm;515nm 548nm;491nm
8 RE; GO GBAFP-GNB1L-03005-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-GNB1L-03005-REGR 599nm;515nm 580nm;491nm

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