Gene-specific Copy Number Variation Probe-PKHD1
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Catalog: |
CNVFP-PKHD1-15744 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PKHD1). 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: |
PKHD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PKHD1 genes. This product achieves the purpose of detection by hybridizing with the PKHD1 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 |
PKHD1, Fibrocystin/polyductin |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is predicted to have a single transmembrane (TM)-spanning domain and multiple copies of an immunoglobulin-like plexin-transcription-factor domain. Alternative splicing results in two transcript variants encoding different isoforms. Other alternatively spliced transcripts have been described, but the full length sequences have not been determined. Several of these transcripts are predicted to encode truncated products which lack the TM and may be secreted. Mutations in this gene cause autosomal recessive polycystic kidney disease, also known as polycystic kidney and hepatic disease-1. [provided by RefSeq, Jul 2008] |
Gene Symbol |
PKHD1 |
Location |
6p12.3-p12.2 |
Chromosome |
Chromosome6 |
Coordinates |
This gene maps to 51480144-51952423 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-PKHD1-15744-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PKHD1-15744-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PKHD1-15744-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PKHD1-15744-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PKHD1-15744-AQ |
467nm |
418nm |
|
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