Gene-specific Copy Number Variation Probe-RBM8A
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Catalog: |
CNVFP-RBM8A-16961 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RBM8A). 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: |
RBM8A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RBM8A genes. This product achieves the purpose of detection by hybridizing with the RBM8A 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 |
RNA Binding Motif Protein 8A |
Gene Summary [Provided by RefSeq] |
This gene encodes a protein with a conserved RNA-binding motif. The protein is found predominantly in the nucleus, although it is also present in the cytoplasm. It is preferentially associated with mRNAs produced by splicing, including both nuclear mRNAs and newly exported cytoplasmic mRNAs. It is thought that the protein remains associated with spliced mRNAs as a tag to indicate where introns had been present, thus coupling pre- and post-mRNA splicing events. Previously, it was thought that two genes encode this protein, RBM8A and RBM8B; it is now thought that the RBM8B locus is a pseudogene. There are two alternate translation start codons with this gene, which result in two forms of the protein. An allele mutation and a low-frequency noncoding single-nucleotide polymorphism (SNP) in this gene cause thrombocytopenia-absent radius (TAR) syndrome. [provided by RefSeq, Jul 2013] |
Gene Symbol |
RBM8A |
Location |
1q21.1 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 145507556-145513535 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-RBM8A-16961-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-RBM8A-16961-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-RBM8A-16961-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-RBM8A-16961-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-RBM8A-16961-AQ |
467nm |
418nm |
|
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