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| Catalog: | GBAFP-SHOX2-07319 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SHOX2). 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: | SHOX2 Gene-specific Break Apart Probe is designed to detect potential SHOX2 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 | Short Stature Homeobox 2 |
| Gene Summary [Provided by RefSeq] | This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009] |
| Gene Symbol | SHOX2 |
| Location | 3q25.32 |
| Chromosome | Chromosome3 |
| Coordinates | This gene maps to 157813799-157823952 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-SHOX2-07319-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-SHOX2-07319-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SHOX2-07319-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SHOX2-07319-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SHOX2-07319-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-SHOX2-07319-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-SHOX2-07319-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-SHOX2-07319-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SHOX2-07319-REGR | 599nm;515nm | 580nm;491nm |
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