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| Catalog: | GBAFP-CD40-10829 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CD40). 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: | CD40 Gene-specific Break Apart Probe is designed to detect potential CD40 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 | CD40 Molecule |
| Gene Summary [Provided by RefSeq] | This gene is a member of the TNF-receptor superfamily. The encoded protein is a receptor on antigen-presenting cells of the immune system and is essential for mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3). Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Nov 2014] |
| Gene Symbol | CD40 |
| Location | 20q13.12 |
| Chromosome | Chromosome20 |
| Coordinates | This gene maps to 44746905-44758384 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-CD40-10829-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-CD40-10829-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CD40-10829-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CD40-10829-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CD40-10829-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-CD40-10829-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-CD40-10829-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-CD40-10829-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CD40-10829-REGR | 599nm;515nm | 580nm;491nm |
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