Gene-specific Copy Number Variation Probe-ALPL
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Catalog: |
CNVFP-ALPL-00541 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ALPL). 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: |
ALPL Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ALPL genes. This product achieves the purpose of detection by hybridizing with the ALPL 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 |
Alkaline Phosphatase, Liver/bone/kidney |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the alkaline phosphatase family of proteins. There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature enzyme. This enzyme may play a role in bone mineralization. Mutations in this gene have been linked to hypophosphatasia, a disorder that is characterized by hypercalcemia and skeletal defects. [provided by RefSeq, Oct 2015] |
Gene Symbol |
ALPL |
Location |
1p36.12 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 21835857-21904905 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-ALPL-00541-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-ALPL-00541-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-ALPL-00541-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-ALPL-00541-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-ALPL-00541-AQ |
467nm |
418nm |
|
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