Gene-specific Copy Number Variation Probe-PLOD2
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| Catalog: |
CNVFP-PLOD2-15984 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PLOD2). 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: |
PLOD2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PLOD2 genes. This product achieves the purpose of detection by hybridizing with the PLOD2 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 |
Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity. Mutations in the coding region of this gene are associated with Bruck syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
PLOD2 |
| Location |
3q24 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 145787227-145879282 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-PLOD2-15984-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PLOD2-15984-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PLOD2-15984-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PLOD2-15984-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PLOD2-15984-AQ |
467nm |
418nm |
|
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