Gene-specific Copy Number Variation Probe-HAMP
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Catalog: |
CNVFP-HAMP-06354 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HAMP). 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: |
HAMP Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HAMP genes. This product achieves the purpose of detection by hybridizing with the HAMP 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 |
Hepcidin Antimicrobial Peptide |
Gene Summary [Provided by RefSeq] |
The product encoded by this gene is involved in the maintenance of iron homeostasis, and it is necessary for the regulation of iron storage in macrophages, and for intestinal iron absorption. The preproprotein is post-translationally cleaved into mature peptides of 20, 22 and 25 amino acids, and these active peptides are rich in cysteines, which form intramolecular bonds that stabilize their beta-sheet structures. These peptides exhibit antimicrobial activity against bacteria and fungi. Mutations in this gene cause hemochromatosis type 2B, also known as juvenile hemochromatosis, a disease caused by severe iron overload that results in cardiomyopathy, cirrhosis, and endocrine failure. [provided by RefSeq, Oct 2014] |
Gene Symbol |
HAMP |
Location |
19q13.12 |
Chromosome |
Chromosome19 |
Coordinates |
This gene maps to 35773409-35776045 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-HAMP-06354-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-HAMP-06354-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-HAMP-06354-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-HAMP-06354-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-HAMP-06354-AQ |
467nm |
418nm |
|
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