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| Catalog: | GBAFP-SFTPB-07367 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SFTPB). 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: | SFTPB Gene-specific Break Apart Probe is designed to detect potential SFTPB 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 | Surfactant Protein B |
| Gene Summary [Provided by RefSeq] | This gene encodes the pulmonary-associated surfactant protein B (SPB), an amphipathic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. The SPB enhances the rate of spreading and increases the stability of surfactant monolayers in vitro. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 1, also called pulmonary alveolar proteinosis due to surfactant protein B deficiency, and are associated with fatal respiratory distress in the neonatal period. Alternatively spliced transcript variants encoding the same protein have been identified.[provided by RefSeq, Feb 2010] |
| Gene Symbol | SFTPB |
| Location | 2p11.2 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 85884439-85895864 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-SFTPB-07367-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-SFTPB-07367-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SFTPB-07367-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SFTPB-07367-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SFTPB-07367-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-SFTPB-07367-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-SFTPB-07367-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-SFTPB-07367-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SFTPB-07367-REGR | 599nm;515nm | 580nm;491nm |
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