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| Catalog: | GBAFP-MPZ-05112 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (MPZ). 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: | MPZ Gene-specific Break Apart Probe is designed to detect potential MPZ 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 | Myelin Protein Zero |
| Gene Summary [Provided by RefSeq] | This gene is specifically expressed in Schwann cells of the peripheral nervous system and encodes a type I transmembrane glycoprotein that is a major structural protein of the peripheral myelin sheath. The encoded protein contains a large hydrophobic extracellular domain and a smaller basic intracellular domain, which are essential for the formation and stabilization of the multilamellar structure of the compact myelin. Mutations in this gene are associated with autosomal dominant form of Charcot-Marie-Tooth disease type 1 (CMT1B) and other polyneuropathies, such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN). A recent study showed that two isoforms are produced from the same mRNA by use of alternative in-frame translation termination codons via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2015] |
| Gene Symbol | MPZ |
| Location | 1q23.3 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 161274524-161279762 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-MPZ-05112-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-MPZ-05112-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-MPZ-05112-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-MPZ-05112-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-MPZ-05112-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-MPZ-05112-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-MPZ-05112-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-MPZ-05112-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-MPZ-05112-REGR | 599nm;515nm | 580nm;491nm |
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