Gene-specific Copy Number Variation Probe-FAM111A
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| Catalog: |
CNVFP-FAM111A-04895 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FAM111A). 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: |
FAM111A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FAM111A genes. This product achieves the purpose of detection by hybridizing with the FAM111A 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 |
Family With Sequence Similarity 111 Member A |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is cell-cycle regulated, and has nuclear localization. The C-terminal half of the protein shares homology with trypsin-like peptidases and it contains a PCNA-interacting peptide (PIP) box, that is necessary for its co-localization with proliferating cell nuclear antigen (PCNA). Reduced expression of this gene resulted in DNA replication defects, consistent with the demonstrated role for this gene in Simian Virus 40 (SV40) viral replication. Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS, also known as Gracile Bone Dysplasia), both characterized by short stature, hypoparathyroidism, bone development abnormalities, and hypocalcemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |
| Gene Symbol |
FAM111A |
| Location |
11q12.1 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 58910317-58922511 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-FAM111A-04895-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FAM111A-04895-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FAM111A-04895-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FAM111A-04895-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FAM111A-04895-AQ |
467nm |
418nm |
|
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