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Gene-specific Copy Number Variation Probe-RAP1GAP

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Catalog: CNVFP-RAP1GAP-17056
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RAP1GAP). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services.
Application: RAP1GAP Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RAP1GAP genes. This product achieves the purpose of detection by hybridizing with the RAP1GAP gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH.
Category: Copy Number Variation
Probe Kits Volume (µL): 40 μL
Quantity: 20 Tests
Hybridization Solution (µL): 200 μL
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping
Storage Conditions: Store at -20℃ and avoid light;
Shipping Conditions: -20℃

Gene Details

Gene Name RAP1 GTPase Activating Protein
Gene Summary [Provided by RefSeq] This gene encodes a type of GTPase-activating-protein (GAP) that down-regulates the activity of the ras-related RAP1 protein. RAP1 acts as a molecular switch by cycling between an inactive GDP-bound form and an active GTP-bound form. The product of this gene, RAP1GAP, promotes the hydrolysis of bound GTP and hence returns RAP1 to the inactive state whereas other proteins, guanine nucleotide exchange factors (GEFs), act as RAP1 activators by facilitating the conversion of RAP1 from the GDP- to the GTP-bound form. In general, ras subfamily proteins, such as RAP1, play key roles in receptor-linked signaling pathways that control cell growth and differentiation. RAP1 plays a role in diverse processes such as cell proliferation, adhesion, differentiation, and embryogenesis. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Aug 2011]
Gene Symbol RAP1GAP
Location 1p36.12
Chromosome Chromosome1
Coordinates This gene maps to 21922707-21995856 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-RAP1GAP-17056-OR 573nm 548nm
2 RE CNVFP-RAP1GAP-17056-RE 599nm 580nm
3 GO CNVFP-RAP1GAP-17056-GO 551nm 525nm
4 GR CNVFP-RAP1GAP-17056-GR 515nm 491nm
5 AQ CNVFP-RAP1GAP-17056-AQ 467nm 418nm

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