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| Catalog: | GBAFP-CHRNG-11035 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CHRNG). 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: | CHRNG Gene-specific Break Apart Probe is designed to detect potential CHRNG 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 | Cholinergic Receptor Nicotinic Gamma Subunit |
| Gene Summary [Provided by RefSeq] | The mammalian muscle-type acetylcholine receptor is a transmembrane pentameric glycoprotein with two alpha subunits, one beta, one delta, and one epsilon (in adult skeletal muscle) or gamma (in fetal and denervated muscle) subunit. This gene, which encodes the gamma subunit, is expressed prior to the thirty-third week of gestation in humans. The gamma subunit of the acetylcholine receptor plays a role in neuromuscular organogenesis and ligand binding and disruption of gamma subunit expression prevents the correct localization of the receptor in cell membranes. Mutations in this gene cause Escobar syndrome and a lethal form of multiple pterygium syndrome. Muscle-type acetylcholine receptor is the major antigen in the autoimmune disease myasthenia gravis.[provided by RefSeq, Sep 2009] |
| Gene Symbol | CHRNG |
| Location | 2q37.1 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 233404436-233411038 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-CHRNG-11035-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-CHRNG-11035-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CHRNG-11035-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CHRNG-11035-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CHRNG-11035-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-CHRNG-11035-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-CHRNG-11035-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-CHRNG-11035-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CHRNG-11035-REGR | 599nm;515nm | 580nm;491nm |
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