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| Catalog: | GBAFP-NRXN1-05664 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NRXN1). 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: | NRXN1 Gene-specific Break Apart Probe is designed to detect potential NRXN1 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 | Neurexin 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a single-pass type I membrane protein that belongs to the neurexin family. Neurexins are cell-surface receptors that bind neuroligins to form Ca(2+)-dependent neurexin/neuroligin complexes at synapses in the central nervous system. This complex is required for efficient neurotransmission and is involved in the formation of synaptic contacts. Three members of this gene family have been studied in detail and are estimated to generate over 3,000 variants through the use of two alternative promoters (alpha and beta) and extensive alternative splicing in each family member. Recently, a third promoter (gamma) was identified for this gene in the 3' region. Mutations in this gene are associated with Pitt-Hopkins-like syndrome-2 and may contribute to susceptibility to schizophrenia. [provided by RefSeq, Aug 2016] |
| Gene Symbol | NRXN1 |
| Location | 2p16.3 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 50145642-51259674 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-NRXN1-05664-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-NRXN1-05664-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-NRXN1-05664-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-NRXN1-05664-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-NRXN1-05664-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-NRXN1-05664-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-NRXN1-05664-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-NRXN1-05664-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-NRXN1-05664-REGR | 599nm;515nm | 580nm;491nm |
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