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| Catalog: | GBAFP-GLI2-12450 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (GLI2). 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: | GLI2 Gene-specific Break Apart Probe is designed to detect potential GLI2 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 | GLI Family Zinc Finger 2 |
| Gene Summary [Provided by RefSeq] | This gene encodes a protein which belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as transcription factors which bind DNA through zinc finger motifs. These motifs contain conserved H-C links. Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in the embryonal carcinoma cell. The protein encoded by this gene localizes to the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008] |
| Gene Symbol | GLI2 |
| Location | 2q14.2 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 121554866-121750229 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-GLI2-12450-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-GLI2-12450-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-GLI2-12450-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-GLI2-12450-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-GLI2-12450-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-GLI2-12450-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-GLI2-12450-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-GLI2-12450-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-GLI2-12450-REGR | 599nm;515nm | 580nm;491nm |
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