Gene-specific Copy Number Variation Probe-CSH1
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| Catalog: |
CNVFP-CSH1-03264 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CSH1). 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: |
CSH1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CSH1 genes. This product achieves the purpose of detection by hybridizing with the CSH1 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 |
Chorionic Somatomammotropin Hormone 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. The gene is located at the growth hormone locus on chromosome 17 along with four other related genes in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. This particular family member is expressed mainly in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, although the ratio of 1 to 2 increases by term. Mutations in this gene result in placental lactogen deficiency and Silver-Russell syndrome. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
CSH1 |
| Location |
17q23.3 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 61972267-61974021 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-CSH1-03264-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CSH1-03264-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CSH1-03264-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CSH1-03264-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CSH1-03264-AQ |
467nm |
418nm |
|
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