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| Catalog: | GBAFP-ABCC2-09571 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ABCC2). 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: | ABCC2 Gene-specific Break Apart Probe is designed to detect potential ABCC2 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 | ATP Binding Cassette Subfamily C Member 2 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport. Substrates include anticancer drugs such as vinblastine; therefore, this protein appears to contribute to drug resistance in mammalian cells. Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. [provided by RefSeq, Jul 2008] |
| Gene Symbol | ABCC2 |
| Location | 10q24.2 |
| Chromosome | Chromosome10 |
| Coordinates | This gene maps to 101542462-101611662 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-ABCC2-09571-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-ABCC2-09571-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ABCC2-09571-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ABCC2-09571-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ABCC2-09571-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-ABCC2-09571-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-ABCC2-09571-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-ABCC2-09571-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ABCC2-09571-REGR | 599nm;515nm | 580nm;491nm |
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