Gene-specific Copy Number Variation Probe-ASPH
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| Catalog: |
CNVFP-ASPH-00929 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ASPH). 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: |
ASPH Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ASPH genes. This product achieves the purpose of detection by hybridizing with the ASPH 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 |
Aspartate Beta-hydroxylase |
| Gene Summary [Provided by RefSeq] |
This gene is thought to play an important role in calcium homeostasis. The gene is expressed from two promoters and undergoes extensive alternative splicing. The encoded set of proteins share varying amounts of overlap near their N-termini but have substantial variations in their C-terminal domains resulting in distinct functional properties. The longest isoforms (a and f) include a C-terminal Aspartyl/Asparaginyl beta-hydroxylase domain that hydroxylates aspartic acid or asparagine residues in the epidermal growth factor (EGF)-like domains of some proteins, including protein C, coagulation factors VII, IX, and X, and the complement factors C1R and C1S. Other isoforms differ primarily in the C-terminal sequence and lack the hydroxylase domain, and some have been localized to the endoplasmic and sarcoplasmic reticulum. Some of these isoforms are found in complexes with calsequestrin, triadin, and the ryanodine receptor, and have been shown to regulate calcium release from the sarcoplasmic reticulum. Some isoforms have been implicated in metastasis. [provided by RefSeq, Sep 2009] |
| Gene Symbol |
ASPH |
| Location |
8q12.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 62413114-62627199 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-ASPH-00929-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ASPH-00929-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ASPH-00929-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ASPH-00929-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ASPH-00929-AQ |
467nm |
418nm |
|
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