banner
  • Home
  • Gene-specific Copy Number Variation Probe-PTH1R

Gene-specific Copy Number Variation Probe-PTH1R

Add to Cart
Catalog: CNVFP-PTH1R-16703
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PTH1R). 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: PTH1R Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PTH1R genes. This product achieves the purpose of detection by hybridizing with the PTH1R 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 Parathyroid Hormone 1 Receptor
Gene Summary [Provided by RefSeq] The protein encoded by this gene is a member of the G-protein coupled receptor family 2. This protein is a receptor for parathyroid hormone (PTH) and for parathyroid hormone-like hormone (PTHLH). The activity of this receptor is mediated by G proteins which activate adenylyl cyclase and also a phosphatidylinositol-calcium second messenger system. Defects in this receptor are known to be the cause of Jansen's metaphyseal chondrodysplasia (JMC), chondrodysplasia Blomstrand type (BOCD), as well as enchodromatosis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]
Gene Symbol PTH1R
Location 3p21.31
Chromosome Chromosome3
Coordinates This gene maps to 46919235-46945289 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-PTH1R-16703-OR 573nm 548nm
2 RE CNVFP-PTH1R-16703-RE 599nm 580nm
3 GO CNVFP-PTH1R-16703-GO 551nm 525nm
4 GR CNVFP-PTH1R-16703-GR 515nm 491nm
5 AQ CNVFP-PTH1R-16703-AQ 467nm 418nm

Other Products

Online Inquiry

Order

0
Inquiry Basket ( 0 ) Choose Dye*