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Gene-specific Break Apart Probe-MC1R

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Catalog: GBAFP-MC1R-13893
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (MC1R). 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: MC1R Gene-specific Break Apart Probe is designed to detect potential MC1R 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 Details

Gene Name Melanocortin 1 Receptor
Gene Summary [Provided by RefSeq] This intronless gene encodes the receptor protein for melanocyte-stimulating hormone (MSH). The encoded protein, a seven pass transmembrane G protein coupled receptor, controls melanogenesis. Two types of melanin exist: red pheomelanin and black eumelanin. Gene mutations that lead to a loss in function are associated with increased pheomelanin production, which leads to lighter skin and hair color. Eumelanin is photoprotective but pheomelanin may contribute to UV-induced skin damage by generating free radicals upon UV radiation. Binding of MSH to its receptor activates the receptor and stimulates eumelanin synthesis. This receptor is a major determining factor in sun sensitivity and is a genetic risk factor for melanoma and non-melanoma skin cancer. Over 30 variant alleles have been identified which correlate with skin and hair color, providing evidence that this gene is an important component in determining normal human pigment variation. [provided by RefSeq, Jul 2008]
Gene Symbol MC1R
Location 16q24.3
Chromosome Chromosome16
Coordinates This gene maps to 89984286-89987385 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR; GR GBAFP-MC1R-13893-ORGR 573nm;515nm 548nm;491nm
2 AQ; OR GBAFP-MC1R-13893-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-MC1R-13893-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-MC1R-13893-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-MC1R-13893-GRGO 515nm;551nm 491nm;525nm
6 GR; OR GBAFP-MC1R-13893-GROR 515nm;573nm 491nm;548nm
7 GR; RE GBAFP-MC1R-13893-GRRE 515nm;599nm 491nm;580nm
8 RE; GO GBAFP-MC1R-13893-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-MC1R-13893-REGR 599nm;515nm 580nm;491nm

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