Gene-specific Copy Number Variation Probe-PRSS2
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Catalog: |
CNVFP-PRSS2-16486 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRSS2). 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: |
PRSS2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRSS2 genes. This product achieves the purpose of detection by hybridizing with the PRSS2 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 |
Protease, Serine 2 |
Gene Summary [Provided by RefSeq] |
This gene belongs to the trypsin family of serine proteases and encodes anionic trypsinogen. It is part of a cluster of trypsinogen genes that are located within the T cell receptor beta locus. Enzymes of this family cleave peptide bonds that follow lysine or arginine residues. This protein is found at high levels in pancreatic juice and its upregulation is a characteristic feature of pancreatitis. This protein has also been found to activate pro-urokinase in ovarian tumors, suggesting a function in tumor invasion. In addition, this enzyme is able to cleave across the type II collagen triple helix in rheumatoid arthritis synovitis tissue, potentially participating in the degradation of type II collagen-rich cartilage matrix. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2015] |
Gene Symbol |
PRSS2 |
Location |
7q34 |
Chromosome |
Chromosome7 |
Coordinates |
This gene maps to 142479907-142481378 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
1 |
OR
|
CNVFP-PRSS2-16486-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PRSS2-16486-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PRSS2-16486-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PRSS2-16486-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PRSS2-16486-AQ |
467nm |
418nm |
|
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