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| Catalog: | GBAFP-SYNGAP1-17849 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SYNGAP1). 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: | SYNGAP1 Gene-specific Break Apart Probe is designed to detect potential SYNGAP1 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 | Synaptic Ras GTPase Activating Protein 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a Ras GTPase activating protein that is a member of the N-methyl-D-aspartate receptor complex. The N-terminal domain of the protein contains a Ras-GAP domain, a pleckstrin homology domain, and a C2 domain that may be involved in binding of calcium and phospholipids. The C-terminal domain consists of a ten histidine repeat region, serine and tyrosine phosphorylation sites, and a T/SXV motif required for postsynaptic scaffold protein interaction. The encoded protein negatively regulates Ras, Rap and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor trafficking to the postsynaptic membrane to regulate synaptic plasticity and neuronal homeostasis. Allelic variants of this gene are associated with intellectual disability and autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016] |
| Gene Symbol | SYNGAP1 |
| Location | 6p21.32 |
| Chromosome | Chromosome6 |
| Coordinates | This gene maps to 33387846-33421466 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-SYNGAP1-17849-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-SYNGAP1-17849-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SYNGAP1-17849-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SYNGAP1-17849-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SYNGAP1-17849-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-SYNGAP1-17849-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-SYNGAP1-17849-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-SYNGAP1-17849-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SYNGAP1-17849-REGR | 599nm;515nm | 580nm;491nm |
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