CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-F11-11997 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (F11). 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: | F11 Gene-specific Break Apart Probe is designed to detect potential F11 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 | coagulation factor XI |
| Gene Summary [Provided by RefSeq] | This gene encodes coagulation factor XI of the blood coagulation cascade. This protein is present in plasma as a zymogen, which is a unique plasma coagulation enzyme because it exists as a homodimer consisting of two identical polypeptide chains linked by disulfide bonds. During activation of the plasma factor XI, an internal peptide bond is cleaved by factor XIIa (or XII) in each of the two chains, resulting in activated factor XIa, a serine protease composed of two heavy and two light chains held together by disulfide bonds. This activated plasma factor XI triggers the middle phase of the intrisic pathway of blood coagulation by activating factor IX. Defects in this factor lead to Rosenthal syndrome, a blood coagulation abnormality. [provided by RefSeq, Jul 2008] |
| Gene Symbol | F11 |
| Location | 4q35.2 |
| Chromosome | Chromosome4 |
| Coordinates | This gene maps to 187187343-187210835 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-F11-11997-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-F11-11997-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-F11-11997-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-F11-11997-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-F11-11997-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-F11-11997-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-F11-11997-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-F11-11997-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-F11-11997-REGR | 599nm;515nm | 580nm;491nm |
Other Products