Gene-specific Copy Number Variation Probe-LOXL1
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| Catalog: |
CNVFP-LOXL1-10478 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (LOXL1). 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: |
LOXL1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to LOXL1 genes. This product achieves the purpose of detection by hybridizing with the LOXL1 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 |
Lysyl Oxidase Like 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome. [provided by RefSeq, Jan 2016] |
| Gene Symbol |
LOXL1 |
| Location |
15q24.1 |
| Chromosome |
Chromosome15 |
| Coordinates |
This gene maps to 74218788-74244478 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-LOXL1-10478-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-LOXL1-10478-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-LOXL1-10478-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-LOXL1-10478-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-LOXL1-10478-AQ |
467nm |
418nm |
|
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