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| Catalog: | GBAFP-AMH-09783 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (AMH). 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: | AMH Gene-specific Break Apart Probe is designed to detect potential AMH 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 | Anti-Mullerian Hormone |
| Gene Summary [Provided by RefSeq] | This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate N- and C-terminal cleavage products that homodimerize and associate to form a biologically active noncovalent complex. This complex binds to the anti-Mullerian hormone receptor type 2 and causes the regression of Mullerian ducts in the male embryo that would otherwise differentiate into the uterus and fallopian tubes. This protein also plays a role in Leydig cell differentiation and function and follicular development in adult females. Mutations in this gene result in persistent Mullerian duct syndrome. [provided by RefSeq, Jul 2016] |
| Gene Symbol | AMH |
| Location | 19p13.3 |
| Chromosome | Chromosome19 |
| Coordinates | This gene maps to 2249112-2252072 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-AMH-09783-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-AMH-09783-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-AMH-09783-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-AMH-09783-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-AMH-09783-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-AMH-09783-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-AMH-09783-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-AMH-09783-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-AMH-09783-REGR | 599nm;515nm | 580nm;491nm |
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