Gene-specific Copy Number Variation Probe-ACP2
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| Catalog: |
CNVFP-ACP2-00008 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ACP2). 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: |
ACP2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ACP2 genes. This product achieves the purpose of detection by hybridizing with the ACP2 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 |
| 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 |
Acid Phosphatase 2, Lysosomal |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to the histidine acid phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell acid phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene in mice showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2017] |
| Gene Symbol |
ACP2 |
| Location |
11p12-p11 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 47260852-47270457 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-ACP2-00008-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ACP2-00008-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ACP2-00008-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ACP2-00008-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ACP2-00008-AQ |
467nm |
418nm |
|
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