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| Catalog: | GBAFP-CEP104-01346 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CEP104). 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: | CEP104 Gene-specific Break Apart Probe is designed to detect potential CEP104 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 | Centrosomal Protein 104 |
| Gene Summary [Provided by RefSeq] | This gene encodes a centrosomal protein required for ciliogenesis and for ciliary tip structural integrity. The mammalian protein contains three amino-terminal hydrophobic domains, two glycosylation sites, four cysteine-rich motifs, and two regions with homology to the glutamate receptor ionotropic, NMDA 1 protein. During ciliogenesis, the encoded protein translocates from the distal tips of the centrioles to the tip of the elongating cilium. Knockdown of the protein in human retinal pigment cells results in severe defects in ciliogenesis with structural deformities at the ciliary tips. Allelic variants of this gene are associated with the autosomal-recessive disorder Joubert syndrome, which is characterized by a distinctive mid-hindbrain and cerebellar malformation, oculomotor apraxia, irregular breathing, developmental delay, and ataxia. [provided by RefSeq, Feb 2016] |
| Gene Symbol | CEP104 |
| Location | 1p36.32 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 3728644-3773797 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-CEP104-01346-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-CEP104-01346-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CEP104-01346-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CEP104-01346-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CEP104-01346-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-CEP104-01346-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-CEP104-01346-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-CEP104-01346-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CEP104-01346-REGR | 599nm;515nm | 580nm;491nm |
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