Gene-specific Copy Number Variation Probe-COL18A1
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| Catalog: |
CNVFP-COL18A1-02885 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (COL18A1). 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: |
COL18A1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to COL18A1 genes. This product achieves the purpose of detection by hybridizing with the COL18A1 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 |
Collagen Type XVIII Alpha 1 Chain |
| Gene Summary [Provided by RefSeq] |
This gene encodes the alpha chain of type XVIII collagen. This collagen is one of the multiplexins, extracellular matrix proteins that contain multiple triple-helix domains (collagenous domains) interrupted by non-collagenous domains. A long isoform of the protein has an N-terminal domain that is homologous to the extracellular part of frizzled receptors. Proteolytic processing at several endogenous cleavage sites in the C-terminal domain results in production of endostatin, a potent antiangiogenic protein that is able to inhibit angiogenesis and tumor growth. Mutations in this gene are associated with Knobloch syndrome. The main features of this syndrome involve retinal abnormalities, so type XVIII collagen may play an important role in retinal structure and in neural tube closure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
| Gene Symbol |
COL18A1 |
| Location |
21q22.3 |
| Chromosome |
Chromosome21 |
| Coordinates |
This gene maps to 46825096-46933634 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-COL18A1-02885-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-COL18A1-02885-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-COL18A1-02885-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-COL18A1-02885-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-COL18A1-02885-AQ |
467nm |
418nm |
|
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