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Gene-specific Copy Number Variation Probe-PAEP

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Catalog: CNVFP-PAEP-15349
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PAEP). 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: PAEP Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PAEP genes. This product achieves the purpose of detection by hybridizing with the PAEP 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 Progestagen Associated Endometrial Protein
Gene Summary [Provided by RefSeq] This gene is a member of the kernel lipocalin superfamily whose members share relatively low sequence similarity but have highly conserved exon/intron structure and three-dimensional protein folding. Most lipocalins are clustered on the long arm of chromosome 9. The encoded glycoprotein has been previously referred to as pregnancy-associated endometrial alpha-2-globulin, placental protein 14, and glycodelin, but has been officially named progestagen-associated endometrial protein. Three distinct forms, with identical protein backbones but different glycosylation profiles, are found in amniotic fluid, follicular fluid and seminal plasma of the reproductive system. These glycoproteins have distinct and essential roles in regulating a uterine environment suitable for pregnancy and in the timing and occurrence of the appropriate sequence of events in the fertilization process. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]
Gene Symbol PAEP
Location 9q34.3
Chromosome Chromosome9
Coordinates This gene maps to 138453603-138458622 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-PAEP-15349-OR 573nm 548nm
2 RE CNVFP-PAEP-15349-RE 599nm 580nm
3 GO CNVFP-PAEP-15349-GO 551nm 525nm
4 GR CNVFP-PAEP-15349-GR 515nm 491nm
5 AQ CNVFP-PAEP-15349-AQ 467nm 418nm

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