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| Catalog: | GBAFP-PLIN2-06228 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PLIN2). 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: | PLIN2 Gene-specific Break Apart Probe is designed to detect potential PLIN2 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 | Perilipin 2 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene belongs to the perilipin family, members of which coat intracellular lipid storage droplets. This protein is associated with the lipid globule surface membrane material, and maybe involved in development and maintenance of adipose tissue. However, it is not restricted to adipocytes as previously thought, but is found in a wide range of cultured cell lines, including fibroblasts, endothelial and epithelial cells, and tissues, such as lactating mammary gland, adrenal cortex, Sertoli and Leydig cells, and hepatocytes in alcoholic liver cirrhosis, suggesting that it may serve as a marker of lipid accumulation in diverse cell types and diseases. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2011] |
| Gene Symbol | PLIN2 |
| Location | 9p22.1 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 19115758-19127604 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-PLIN2-06228-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-PLIN2-06228-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PLIN2-06228-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PLIN2-06228-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PLIN2-06228-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-PLIN2-06228-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-PLIN2-06228-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-PLIN2-06228-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PLIN2-06228-REGR | 599nm;515nm | 580nm;491nm |
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