Gene-specific Copy Number Variation Probe-NBPF14
Add to Cart
| Catalog: |
CNVFP-NBPF14-13884 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NBPF14). 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: |
NBPF14 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NBPF14 genes. This product achieves the purpose of detection by hybridizing with the NBPF14 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 |
NBPF Member 14 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, May 2013] |
| Gene Symbol |
NBPF14 |
| Location |
1q21.2 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 148003641-148025848 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-NBPF14-13884-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NBPF14-13884-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NBPF14-13884-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NBPF14-13884-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NBPF14-13884-AQ |
467nm |
418nm |
|
Other Products
