Gene-specific Copy Number Variation Probe-PGC
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Catalog: |
CNVFP-PGC-15591 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PGC). 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: |
PGC Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PGC genes. This product achieves the purpose of detection by hybridizing with the PGC 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 |
Progastricsin |
Gene Summary [Provided by RefSeq] |
This gene encodes an aspartic proteinase that belongs to the peptidase family A1. The encoded protein is a digestive enzyme that is produced in the stomach and constitutes a major component of the gastric mucosa. This protein is also secreted into the serum. This protein is synthesized as an inactive zymogen that includes a highly basic prosegment. This enzyme is converted into its active mature form at low pH by sequential cleavage of the prosegment that is carried out by the enzyme itself. Polymorphisms in this gene are associated with susceptibility to gastric cancers. Serum levels of this enzyme are used as a biomarker for certain gastric diseases including Helicobacter pylori related gastritis. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 1. [provided by RefSeq, Oct 2009] |
Gene Symbol |
PGC |
Location |
6p21.1 |
Chromosome |
Chromosome6 |
Coordinates |
This gene maps to 41704448-41715139 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-PGC-15591-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PGC-15591-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PGC-15591-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PGC-15591-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PGC-15591-AQ |
467nm |
418nm |
|
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