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Gene-specific Copy Number Variation Probe-SNORC

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Catalog: CNVFP-SNORC-19136
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNORC). 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: SNORC Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNORC genes. This product achieves the purpose of detection by hybridizing with the SNORC 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 Secondary Ossification Center Associated Regulator Of Chondrocyte Maturation
Gene Summary [Provided by RefSeq] The Secondary Ossification Center Associated Regulator Of Chondrocyte Maturation (SNORC) gene is located on chr2:232865677 -232878699 at 2q37.1.
Gene Symbol SNORC
Location 2q37.1
Chromosome Chromosome2
Coordinates This gene maps to 232865677-232878699 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-SNORC-19136-OR 573nm 548nm
2 RE CNVFP-SNORC-19136-RE 599nm 580nm
3 GO CNVFP-SNORC-19136-GO 551nm 525nm
4 GR CNVFP-SNORC-19136-GR 515nm 491nm
5 AQ CNVFP-SNORC-19136-AQ 467nm 418nm

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