Gene-specific Copy Number Variation Probe-PKD1
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| Catalog: |
CNVFP-PKD1-15753 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PKD1). 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: |
PKD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PKD1 genes. This product achieves the purpose of detection by hybridizing with the PKD1 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 |
Polycystin 1, Transient Receptor Potential Channel Interacting |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the polycystin protein family. The encoded glycoprotein contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail. It is an integral membrane protein that functions as a regulator of calcium permeable cation channels and intracellular calcium homoeostasis. It is also involved in cell-cell/matrix interactions and may modulate G-protein-coupled signal-transduction pathways. It plays a role in renal tubular development, and mutations in this gene cause autosomal dominant polycystic kidney disease type 1 (ADPKD1). ADPKD1 is characterized by the growth of fluid-filled cysts that replace normal renal tissue and result in end-stage renal failure. Splice variants encoding different isoforms have been noted for this gene. Also, six pseudogenes, closely linked in a known duplicated region on chromosome 16p, have been described. [provided by RefSeq, Oct 2008] |
| Gene Symbol |
PKD1 |
| Location |
16p13.3 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 2138710-2185899 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-PKD1-15753-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PKD1-15753-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PKD1-15753-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PKD1-15753-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PKD1-15753-AQ |
467nm |
418nm |
|
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