Gene-specific Copy Number Variation Probe-HNRNPH2
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| Catalog: |
CNVFP-HNRNPH2-06734 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HNRNPH2). 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: |
HNRNPH2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HNRNPH2 genes. This product achieves the purpose of detection by hybridizing with the HNRNPH2 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 |
Heterogeneous Nuclear Ribonucleoprotein H2 |
| Gene Summary [Provided by RefSeq] |
This gene belongs to the 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 three repeats of quasi-RRM domains that binds to RNAs. It is very similar to the family member HNRPH1. This gene is thought to be involved in Fabray disease and X-linked agammaglobulinemia phenotype. Alternative splicing results in multiple transcript variants encoding the same protein. Read-through transcription between this locus and the ribosomal protein L36a gene has been observed. [provided by RefSeq, Jan 2011] |
| Gene Symbol |
HNRNPH2 |
| Location |
Xq22.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 100663120-100669128 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-HNRNPH2-06734-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HNRNPH2-06734-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HNRNPH2-06734-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HNRNPH2-06734-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HNRNPH2-06734-AQ |
467nm |
418nm |
|
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