Gene-specific Copy Number Variation Probe-EPHB2
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| Catalog: |
CNVFP-EPHB2-04519 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (EPHB2). 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: |
EPHB2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to EPHB2 genes. This product achieves the purpose of detection by hybridizing with the EPHB2 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 |
EPH Receptor B2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the Eph receptor family of receptor tyrosine kinase transmembrane glycoproteins. These receptors are composed of an N-terminal glycosylated ligand-binding domain, a transmembrane region and an intracellular kinase domain. They bind ligands called ephrins and are involved in diverse cellular processes including motility, division, and differentiation. A distinguishing characteristic of Eph-ephrin signaling is that both receptors and ligands are competent to transduce a signaling cascade, resulting in bidirectional signaling. This protein belongs to a subgroup of the Eph receptors called EphB. Proteins of this subgroup are distinguished from other members of the family by sequence homology and preferential binding affinity for membrane-bound ephrin-B ligands. Allelic variants are associated with prostate and brain cancer susceptibility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2015] |
| Gene Symbol |
EPHB2 |
| Location |
1p36.12 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 23037330-23241823 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-EPHB2-04519-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-EPHB2-04519-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-EPHB2-04519-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-EPHB2-04519-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-EPHB2-04519-AQ |
467nm |
418nm |
|
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