Gene-specific Copy Number Variation Probe-FCGR3A
Add to Cart
Catalog: |
CNVFP-FCGR3A-05254 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FCGR3A). 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: |
FCGR3A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FCGR3A genes. This product achieves the purpose of detection by hybridizing with the FCGR3A 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 |
Fc Fragment Of IgG Receptor IIIa |
Gene Summary [Provided by RefSeq] |
This gene encodes a receptor for the Fc portion of immunoglobulin G, and it is involved in the removal of antigen-antibody complexes from the circulation, as well as other other antibody-dependent responses. This gene (FCGR3A) is highly similar to another nearby gene (FCGR3B) located on chromosome 1. The receptor encoded by this gene is expressed on natural killer (NK) cells as an integral membrane glycoprotein anchored through a transmembrane peptide, whereas FCGR3B is expressed on polymorphonuclear neutrophils (PMN) where the receptor is anchored through a phosphatidylinositol (PI) linkage. Mutations in this gene have been linked to susceptibility to recurrent viral infections, susceptibility to systemic lupus erythematosus, and alloimmune neonatal neutropenia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Gene Symbol |
FCGR3A |
Location |
1q23.3 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 161511550-161520413 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-FCGR3A-05254-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-FCGR3A-05254-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-FCGR3A-05254-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-FCGR3A-05254-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-FCGR3A-05254-AQ |
467nm |
418nm |
|
Other Products