Gene-specific Copy Number Variation Probe-RASA1
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| Catalog: |
CNVFP-RASA1-17054 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RASA1). 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: |
RASA1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RASA1 genes. This product achieves the purpose of detection by hybridizing with the RASA1 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 |
RAS P21 Protein Activator 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is located in the cytoplasm and is part of the GAP1 family of GTPase-activating proteins. The gene product stimulates the GTPase activity of normal RAS p21 but not its oncogenic counterpart. Acting as a suppressor of RAS function, the protein enhances the weak intrinsic GTPase activity of RAS proteins resulting in the inactive GDP-bound form of RAS, thereby allowing control of cellular proliferation and differentiation. Mutations leading to changes in the binding sites of either protein are associated with basal cell carcinomas. Mutations also have been associated with hereditary capillary malformations (CM) with or without arteriovenous malformations (AVM) and Parkes Weber syndrome. Alternative splicing results in two isoforms where the shorter isoform, lacking the N-terminal hydrophobic region but retaining the same activity, appears to be abundantly expressed in placental but not adult tissues. [provided by RefSeq, May 2012] |
| Gene Symbol |
RASA1 |
| Location |
5q14.3 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 86564150-86687733 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-RASA1-17054-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RASA1-17054-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RASA1-17054-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RASA1-17054-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RASA1-17054-AQ |
467nm |
418nm |
|
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