Gene-specific Copy Number Variation Probe-PRMT7
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| Catalog: |
CNVFP-PRMT7-16604 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRMT7). 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: |
PRMT7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRMT7 genes. This product achieves the purpose of detection by hybridizing with the PRMT7 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 |
Protein Arginine Methyltransferase 7 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients. [provided by RefSeq, May 2017] |
| Gene Symbol |
PRMT7 |
| Location |
16q22.1 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 68344876-68391169 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-PRMT7-16604-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-PRMT7-16604-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-PRMT7-16604-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-PRMT7-16604-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-PRMT7-16604-AQ |
467nm |
418nm |
|
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