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| Catalog: | GBAFP-IGLL1-03499 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (IGLL1). 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: | IGLL1 Gene-specific Break Apart Probe is designed to detect potential IGLL1 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 | Immunoglobulin Lambda Like Polypeptide 1 |
| Gene Summary [Provided by RefSeq] | The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol | IGLL1 |
| Location | 22q11.23 |
| Chromosome | Chromosome22 |
| Coordinates | This gene maps to 23915312-23922495 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-IGLL1-03499-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-IGLL1-03499-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-IGLL1-03499-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-IGLL1-03499-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-IGLL1-03499-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-IGLL1-03499-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-IGLL1-03499-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-IGLL1-03499-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-IGLL1-03499-REGR | 599nm;515nm | 580nm;491nm |
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