Gene-specific Copy Number Variation Probe-NIPBL
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| Catalog: |
CNVFP-NIPBL-14334 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NIPBL). 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: |
NIPBL Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NIPBL genes. This product achieves the purpose of detection by hybridizing with the NIPBL 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 |
NIPBL, Cohesin Loading Factor |
| Gene Summary [Provided by RefSeq] |
This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins. The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation. It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair. The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat. Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats. Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and cognitive disability. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
NIPBL |
| Location |
5p13.2 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 36876860-37065921 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-NIPBL-14334-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NIPBL-14334-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NIPBL-14334-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NIPBL-14334-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NIPBL-14334-AQ |
467nm |
418nm |
|
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