Gene-specific Copy Number Variation Probe-RBMXL2
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| Catalog: |
CNVFP-RBMXL2-17274 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RBMXL2). 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: |
RBMXL2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RBMXL2 genes. This product achieves the purpose of detection by hybridizing with the RBMXL2 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, X-linked Like 2 |
| Gene Summary [Provided by RefSeq] |
This gene belongs to the HNRPG subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene has two RRM domains that bind RNAs. This gene is intronless and is thought to be derived from a processed retroposon. However, unlike many retroposon-derived genes, this gene is not a pseudogene. The encoded protein has similarity to HNRPG and RBMY proteins and it is suggested to replace HNRPG protein function during meiotic prophase or act as a germ cell-specific splicing regulator. It primarily localizes to the nuclei of meiotic spermatocytes. This gene is a candidate for autosomal male infertility. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
RBMXL2 |
| Location |
11p15.4 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 7110164-7112379 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-RBMXL2-17274-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RBMXL2-17274-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RBMXL2-17274-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RBMXL2-17274-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RBMXL2-17274-AQ |
467nm |
418nm |
|
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