CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-SYN2-17852 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SYN2). 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: | SYN2 Gene-specific Break Apart Probe is designed to detect potential SYN2 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 | Synapsin II |
| Gene Summary [Provided by RefSeq] | This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family encodes a neuron-specific phosphoprotein that selectively binds to small synaptic vesicles in the presynaptic nerve terminal. Polymorphisms in this gene are associated with abnormal presynaptic function and related neuronal disorders, including autism, epilepsy, bipolar disorder and schizophrenia. Alternative splicing of this gene results in multiple transcript variants. The tissue inhibitor of metalloproteinase 4 gene is located within an intron of this gene and is transcribed in the opposite direction. [provided by RefSeq, Feb 2014] |
| Gene Symbol | SYN2 |
| Location | 3p25.2 |
| Chromosome | Chromosome3 |
| Coordinates | This gene maps to 12045861-12233532 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-SYN2-17852-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-SYN2-17852-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SYN2-17852-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SYN2-17852-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SYN2-17852-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-SYN2-17852-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-SYN2-17852-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-SYN2-17852-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SYN2-17852-REGR | 599nm;515nm | 580nm;491nm |
Other Products