Gene-specific Copy Number Variation Probe-GPI
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| Catalog: |
CNVFP-GPI-06291 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GPI). 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: |
GPI Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GPI genes. This product achieves the purpose of detection by hybridizing with the GPI 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 |
Glucose-6-phosphate Isomerase |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the glucose phosphate isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In the cytoplasm, the gene product functions as a glycolytic enzyme (glucose-6-phosphate isomerase) that interconverts glucose-6-phosphate and fructose-6-phosphate. Extracellularly, the encoded protein (also referred to as neuroleukin) functions as a neurotrophic factor that promotes survival of skeletal motor neurons and sensory neurons, and as a lymphokine that induces immunoglobulin secretion. The encoded protein is also referred to as autocrine motility factor based on an additional function as a tumor-secreted cytokine and angiogenic factor. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016] |
| Gene Symbol |
GPI |
| Location |
19q13.11 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 34855644-34893318 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-GPI-06291-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GPI-06291-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GPI-06291-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GPI-06291-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GPI-06291-AQ |
467nm |
418nm |
|
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