Gene-specific Copy Number Variation Probe-H2AFY
Add to Cart
| Catalog: |
CNVFP-H2AFY-06376 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (H2AFY). 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: |
H2AFY Gene-specific copy number variation probes are mainly used to detect the copy number variation related to H2AFY genes. This product achieves the purpose of detection by hybridizing with the H2AFY 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 |
H2A Histone Family Member Y |
| Gene Summary [Provided by RefSeq] |
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a replication-independent histone that is a member of the histone H2A family. It replaces conventional H2A histones in a subset of nucleosomes where it represses transcription and participates in stable X chromosome inactivation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2015] |
| Gene Symbol |
H2AFY |
| Location |
5q31.1 |
| Chromosome |
Chromosome5 |
| Coordinates |
This gene maps to 134670070-134735577 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-H2AFY-06376-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-H2AFY-06376-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-H2AFY-06376-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-H2AFY-06376-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-H2AFY-06376-AQ |
467nm |
418nm |
|
Other Products
