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

Gene-specific Copy Number Variation Probe-PRCP

Add to Cart
Catalog: CNVFP-PRCP-16332
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRCP). 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: PRCP Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRCP genes. This product achieves the purpose of detection by hybridizing with the PRCP 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 Prolylcarboxypeptidase
Gene Summary [Provided by RefSeq] This gene encodes a member of the peptidase S28 family of serine exopeptidases. The encoded preproprotein is proteolytically processed to generate the mature lysosomal prolylcarboxypeptidase. This enzyme cleaves C-terminal amino acids linked to proline in peptides such as angiotension II, III and des-Arg9-bradykinin. The cleavage occurs at acidic pH, but the enzyme activity is retained with some substrates at neutral pH. This enzyme has been shown to be an activator of the cell matrix-associated prekallikrein. The importance of angiotension II, one of the substrates of this enzyme, in regulating blood pressure and electrolyte balance suggests that this gene may be related to essential hypertension. A pseudogene of this gene has been identified on chromosome 2. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016]
Gene Symbol PRCP
Location 11q14.1
Chromosome Chromosome11
Coordinates This gene maps to 82535408-82611557 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-PRCP-16332-OR 573nm 548nm
2 RE CNVFP-PRCP-16332-RE 599nm 580nm
3 GO CNVFP-PRCP-16332-GO 551nm 525nm
4 GR CNVFP-PRCP-16332-GR 515nm 491nm
5 AQ CNVFP-PRCP-16332-AQ 467nm 418nm

Other Products

Online Inquiry

Order

0
Inquiry Basket ( 0 ) Choose Dye*