Gene-specific Copy Number Variation Probe-PTGER4
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| Catalog: |
CNVFP-PTGER4-16717 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PTGER4). 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: |
PTGER4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PTGER4 genes. This product achieves the purpose of detection by hybridizing with the PTGER4 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 |
Prostaglandin E Receptor 4 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the G-protein coupled receptor family. This protein is one of four receptors identified for prostaglandin E2 (PGE2). This receptor can activate T-cell factor signaling. It has been shown to mediate PGE2 induced expression of early growth response 1 (EGR1), regulate the level and stability of cyclooxygenase-2 mRNA, and lead to the phosphorylation of glycogen synthase kinase-3. Knockout studies in mice suggest that this receptor may be involved in the neonatal adaptation of circulatory system, osteoporosis, as well as initiation of skin immune responses. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
PTGER4 |
| Location |
5p13.1 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 40680031-40693837 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-PTGER4-16717-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PTGER4-16717-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PTGER4-16717-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PTGER4-16717-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PTGER4-16717-AQ |
467nm |
418nm |
|
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