Gene-specific Copy Number Variation Probe-PRNP
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Catalog: |
CNVFP-PRNP-16440 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRNP). 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: |
PRNP Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRNP genes. This product achieves the purpose of detection by hybridizing with the PRNP 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 |
Prion Protein |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that tends to aggregate into rod-like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as elsewhere in this gene have been associated with Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler disease, Huntington disease-like 1, and kuru. An overlapping open reading frame has been found for this gene that encodes a smaller, structurally unrelated protein, AltPrp. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014] |
Gene Symbol |
PRNP |
Location |
20p13 |
Chromosome |
Chromosome20 |
Coordinates |
This gene maps to 4666796-4682234 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-PRNP-16440-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PRNP-16440-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PRNP-16440-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PRNP-16440-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PRNP-16440-AQ |
467nm |
418nm |
|
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