Gene-specific Copy Number Variation Probe-H2BFWT
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| Catalog: |
CNVFP-H2BFWT-06371 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (H2BFWT). 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: |
H2BFWT Gene-specific copy number variation probes are mainly used to detect the copy number variation related to H2BFWT genes. This product achieves the purpose of detection by hybridizing with the H2BFWT 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 |
H2B Histone Family Member W, Testis Specific |
| Gene Summary [Provided by RefSeq] |
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene encodes a replication-independent histone that is a member of the H2B histone family that is specifically expressed in sperm nuclei. A polymorphism in the 5' UTR of this gene is associated with male infertility.[provided by RefSeq, Oct 2015] |
| Gene Symbol |
H2BFWT |
| Location |
Xq22.2 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 103265718-103268256 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-H2BFWT-06371-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-H2BFWT-06371-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-H2BFWT-06371-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-H2BFWT-06371-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-H2BFWT-06371-AQ |
467nm |
418nm |
|
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