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| Catalog: | GBAFP-PEX7-15757 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PEX7). 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: | PEX7 Gene-specific Break Apart Probe is designed to detect potential PEX7 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 | Peroxisomal Biogenesis Factor 7 |
| Gene Summary [Provided by RefSeq] | This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq, Oct 2008] |
| Gene Symbol | PEX7 |
| Location | 6q23.3 |
| Chromosome | Chromosome6 |
| Coordinates | This gene maps to 137143701-137235072 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-PEX7-15757-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-PEX7-15757-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PEX7-15757-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PEX7-15757-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PEX7-15757-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-PEX7-15757-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-PEX7-15757-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-PEX7-15757-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PEX7-15757-REGR | 599nm;515nm | 580nm;491nm |
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