Gene-specific Copy Number Variation Probe-PGK1
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| Catalog: |
CNVFP-PGK1-15589 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PGK1). 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: |
PGK1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PGK1 genes. This product achieves the purpose of detection by hybridizing with the PGK1 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 |
Phosphoglycerate Kinase 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a glycolytic enzyme that catalyzes the conversion of 1,3-diphosphoglycerate to 3-phosphoglycerate. The encoded protein may also act as a cofactor for polymerase alpha. Additionally, this protein is secreted by tumor cells where it participates in angiogenesis by functioning to reduce disulfide bonds in the serine protease, plasmin, which consequently leads to the release of the tumor blood vessel inhibitor angiostatin. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Deficiency of the enzyme is associated with a wide range of clinical phenotypes hemolytic anemia and neurological impairment. Pseudogenes of this gene have been defined on chromosomes 19, 21 and the X chromosome. [provided by RefSeq, Jan 2014] |
| Gene Symbol |
PGK1 |
| Location |
Xq21.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 77359665-77382324 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-PGK1-15589-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PGK1-15589-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PGK1-15589-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PGK1-15589-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PGK1-15589-AQ |
467nm |
418nm |
|
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