Gene-specific Copy Number Variation Probe-ACVR2A
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| Catalog: |
CNVFP-ACVR2A-00098 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ACVR2A). 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: |
ACVR2A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ACVR2A genes. This product achieves the purpose of detection by hybridizing with the ACVR2A 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 |
Activin A Receptor Type 2A |
| Gene Summary [Provided by RefSeq] |
This gene encodes a receptor that mediates the functions of activins, which are members of the transforming growth factor-beta (TGF-beta) superfamily involved in diverse biological processes. The encoded protein is a transmembrane serine-threonine kinase receptor which mediates signaling by forming heterodimeric complexes with various combinations of type I and type II receptors and ligands in a cell-specific manner. The encoded type II receptor is primarily involved in ligand-binding and includes an extracellular ligand-binding domain, a transmembrane domain and a cytoplasmic serine-threonine kinase domain. This gene may be associated with susceptibility to preeclampsia, a pregnancy-related disease which can result in maternal and fetal morbidity and mortality. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jun 2013] |
| Gene Symbol |
ACVR2A |
| Location |
2q22.3-q23.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 148602569-148688393 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-ACVR2A-00098-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ACVR2A-00098-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ACVR2A-00098-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ACVR2A-00098-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ACVR2A-00098-AQ |
467nm |
418nm |
|
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