Gene-specific Copy Number Variation Probe-GH2
Add to Cart
| Catalog: |
CNVFP-GH2-05931 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (GH2). 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: |
GH2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to GH2 genes. This product achieves the purpose of detection by hybridizing with the GH2 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 |
Growth Hormone 2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones which play an important role in growth control. The gene, along with four other related genes, is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. The five genes share a remarkably high degree of sequence identity. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. As in the case of its pituitary counterpart, growth hormone 1, the predominant isoform of this particular family member shows similar somatogenic activity, with reduced lactogenic activity. Mutations in this gene lead to placental growth hormone/lactogen deficiency. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
GH2 |
| Location |
17q23.3 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 61957571-61959223 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-GH2-05931-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-GH2-05931-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-GH2-05931-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-GH2-05931-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-GH2-05931-AQ |
467nm |
418nm |
|
Other Products
