Gene-specific Copy Number Variation Probe-SNRNP200
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Catalog: |
CNVFP-SNRNP200-19534 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNRNP200). 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: |
SNRNP200 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNRNP200 genes. This product achieves the purpose of detection by hybridizing with the SNRNP200 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 |
Small Nuclear Ribonucleoprotein U5 Subunit 200 |
Gene Summary [Provided by RefSeq] |
Pre-mRNA splicing is catalyzed by the spliceosome, a complex of specialized RNA and protein subunits that removes introns from a transcribed pre-mRNA segment. The spliceosome consists of small nuclear RNA proteins (snRNPs) U1, U2, U4, U5 and U6, together with approximately 80 conserved proteins. U5 snRNP contains nine specific proteins. This gene encodes one of the U5 snRNP-specific proteins. This protein belongs to the DEXH-box family of putative RNA helicases. It is a core component of U4/U6-U5 snRNPs and appears to catalyze an ATP-dependent unwinding of U4/U6 RNA duplices. Mutations in this gene cause autosomal-dominant retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined. [provided by RefSeq, Mar 2010] |
Gene Symbol |
SNRNP200 |
Location |
2q11.2 |
Chromosome |
Chromosome2 |
Coordinates |
This gene maps to 96940073-96971307 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-SNRNP200-19534-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-SNRNP200-19534-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-SNRNP200-19534-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-SNRNP200-19534-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-SNRNP200-19534-AQ |
467nm |
418nm |
|
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