Gene-specific Copy Number Variation Probe-CEP104
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| Catalog: |
CNVFP-CEP104-02443 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CEP104). 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: |
CEP104 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CEP104 genes. This product achieves the purpose of detection by hybridizing with the CEP104 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 |
Centrosomal Protein 104 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a centrosomal protein required for ciliogenesis and for ciliary tip structural integrity. The mammalian protein contains three amino-terminal hydrophobic domains, two glycosylation sites, four cysteine-rich motifs, and two regions with homology to the glutamate receptor ionotropic, NMDA 1 protein. During ciliogenesis, the encoded protein translocates from the distal tips of the centrioles to the tip of the elongating cilium. Knockdown of the protein in human retinal pigment cells results in severe defects in ciliogenesis with structural deformities at the ciliary tips. Allelic variants of this gene are associated with the autosomal-recessive disorder Joubert syndrome, which is characterized by a distinctive mid-hindbrain and cerebellar malformation, oculomotor apraxia, irregular breathing, developmental delay, and ataxia. [provided by RefSeq, Feb 2016] |
| Gene Symbol |
CEP104 |
| Location |
1p36.32 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 3728644-3773797 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-CEP104-02443-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CEP104-02443-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CEP104-02443-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CEP104-02443-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CEP104-02443-AQ |
467nm |
418nm |
|
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