Gene-specific Copy Number Variation Probe-PTH
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| Catalog: |
CNVFP-PTH-16702 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PTH). 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: |
PTH Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PTH genes. This product achieves the purpose of detection by hybridizing with the PTH 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 |
Parathyroid Hormone |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the parathyroid family of proteins. The encoded preproprotein is proteolytically processed to generate a protein that binds to the parathyroid hormone/parathyroid hormone-related peptide receptor and regulates blood calcium and phosphate levels. Excess production of the encoded protein, known as hyperparathyroidism, can result in hypercalcemia and kidney stones. On the other hand, defective processing of the encoded protein may lead to hypoparathyroidism, which can result in hypocalcemia and numbness. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015] |
| Gene Symbol |
PTH |
| Location |
11p15.3 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 13513600-13517567 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-PTH-16702-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PTH-16702-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PTH-16702-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PTH-16702-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PTH-16702-AQ |
467nm |
418nm |
|
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