Gene-specific Copy Number Variation Probe-DNMT3B
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| Catalog: |
CNVFP-DNMT3B-04135 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DNMT3B). 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: |
DNMT3B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DNMT3B genes. This product achieves the purpose of detection by hybridizing with the DNMT3B 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 |
DNA Methyltransferase 3 Beta |
| Gene Summary [Provided by RefSeq] |
CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined. [provided by RefSeq, May 2011] |
| Gene Symbol |
DNMT3B |
| Location |
20q11.21 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 31350190-31397162 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-DNMT3B-04135-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DNMT3B-04135-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DNMT3B-04135-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DNMT3B-04135-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DNMT3B-04135-AQ |
467nm |
418nm |
|
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