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| Catalog: | GBAFP-SACM1L-16792 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SACM1L). 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: | SACM1L Gene-specific Break Apart Probe is designed to detect potential SACM1L 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 | SAC1 Like Phosphatidylinositide Phosphatase |
| Gene Summary [Provided by RefSeq] | This gene encodes an integral membrane protein, which is localized to the endoplasmic reticulum, and functions as a phosphoinositide phosphatase that hydrolyzes phosphatidylinositol 3-phosphate, phosphatidylinositol 4-phosphate, and phosphatidylinositol 3,5-bisphosphate. Deletion of this gene in mouse results in preimplantation lethality. Other studies suggest that this gene is also involved in the organization of golgi membranes and mitotic spindles. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame, downstream translation termination codon via a stop codon readthrough mechanism.[provided by RefSeq, Dec 2017] |
| Gene Symbol | SACM1L |
| Location | 3p21.31 |
| Chromosome | Chromosome3 |
| Coordinates | This gene maps to 45730753-45786900 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-SACM1L-16792-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-SACM1L-16792-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SACM1L-16792-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SACM1L-16792-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SACM1L-16792-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-SACM1L-16792-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-SACM1L-16792-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-SACM1L-16792-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SACM1L-16792-REGR | 599nm;515nm | 580nm;491nm |
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