Gene-specific Copy Number Variation Probe-GNRHR
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| Catalog: |
CNVFP-GNRHR-06099 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GNRHR). 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: |
GNRHR Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GNRHR genes. This product achieves the purpose of detection by hybridizing with the GNRHR 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 |
Gonadotropin Releasing Hormone Receptor |
| Gene Summary [Provided by RefSeq] |
This gene encodes the receptor for type 1 gonadotropin-releasing hormone. This receptor is a member of the seven-transmembrane, G-protein coupled receptor (GPCR) family. It is expressed on the surface of pituitary gonadotrope cells as well as lymphocytes, breast, ovary, and prostate. Following binding of gonadotropin-releasing hormone, the receptor associates with G-proteins that activate a phosphatidylinositol-calcium second messenger system. Activation of the receptor ultimately causes the release of gonadotropic luteinizing hormone (LH) and follicle stimulating hormone (FSH). Defects in this gene are a cause of hypogonadotropic hypogonadism (HH). Alternative splicing results in multiple transcript variants encoding different isoforms. More than 18 transcription initiation sites in the 5' region and multiple polyA signals in the 3' region have been identified for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
GNRHR |
| Location |
4q13.2 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 68603098-68621804 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-GNRHR-06099-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GNRHR-06099-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GNRHR-06099-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GNRHR-06099-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GNRHR-06099-AQ |
467nm |
418nm |
|
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