Gene-specific Copy Number Variation Probe-RFC2
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| Catalog: |
CNVFP-RFC2-17192 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RFC2). 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: |
RFC2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RFC2 genes. This product achieves the purpose of detection by hybridizing with the RFC2 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 |
Replication Factor C Subunit 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the activator 1 small subunits family. The elongation of primed DNA templates by DNA polymerase delta and epsilon requires the action of the accessory proteins, proliferating cell nuclear antigen (PCNA) and replication factor C (RFC). Replication factor C, also called activator 1, is a protein complex consisting of five distinct subunits. This gene encodes the 40 kD subunit, which has been shown to be responsible for binding ATP and may help promote cell survival. Disruption of this gene is associated with Williams syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene of this gene has been defined on chromosome 2. [provided by RefSeq, Jul 2013] |
| Gene Symbol |
RFC2 |
| Location |
7q11.23 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 73645831-73668738 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-RFC2-17192-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RFC2-17192-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RFC2-17192-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RFC2-17192-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RFC2-17192-AQ |
467nm |
418nm |
|
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