Gene-specific Copy Number Variation Probe-RHCE
Add to Cart
| Catalog: |
CNVFP-RHCE-17441 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RHCE). 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: |
RHCE Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RHCE genes. This product achieves the purpose of detection by hybridizing with the RHCE 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 |
Rh Blood Group CcEe Antigens |
| Gene Summary [Provided by RefSeq] |
The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene which encodes both the RhC and RhE antigens on a single polypeptide and a second gene which encodes the RhD protein. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. A mutation in this gene results in amorph-type Rh-null disease. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Aug 2016] |
| Gene Symbol |
RHCE |
| Location |
1p36.11 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 25688739-25747363 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-RHCE-17441-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RHCE-17441-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RHCE-17441-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RHCE-17441-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RHCE-17441-AQ |
467nm |
418nm |
|
Other Products
