Gene-specific Copy Number Variation Probe-FANCL
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| Catalog: |
CNVFP-FANCL-05374 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FANCL). 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: |
FANCL Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FANCL genes. This product achieves the purpose of detection by hybridizing with the FANCL 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 |
Fanconi Anemia Complementation Group L |
| Gene Summary [Provided by RefSeq] |
The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group L. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
FANCL |
| Location |
2p16.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 58386377-58468515 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-FANCL-05374-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FANCL-05374-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FANCL-05374-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FANCL-05374-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FANCL-05374-AQ |
467nm |
418nm |
|
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