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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 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 |
| 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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