Gene-specific Copy Number Variation Probe-MT3
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Catalog: |
CNVFP-MT3-13467 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MT3). 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: |
MT3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MT3 genes. This product achieves the purpose of detection by hybridizing with the MT3 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 |
Metallothionein 3 |
Gene Summary [Provided by RefSeq] |
This gene is a member of the metallothionein family of genes. Proteins encoded by this gene family are low in molecular weight, are cysteine-rich, lack aromatic residues, and bind divalent heavy metal ions. This gene family member displays tissue-specific expression, and contains a threonine insert near its N-terminus and a glutamate-rich hexapeptide insert near its C-terminus relative to the proteins encoded by other gene family members. It plays an important role in zinc and copper homeostasis, and is induced under hypoxic conditions. The encoded protein is a growth inhibitory factor, and reduced levels of the protein are observed in the brains of individuals with some metal-linked neurodegenerative disorders such as Alzheimer's disease. [provided by RefSeq, Sep 2017] |
Gene Symbol |
MT3 |
Location |
16q13 |
Chromosome |
Chromosome16 |
Coordinates |
This gene maps to 56623266-56625000 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-MT3-13467-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-MT3-13467-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-MT3-13467-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-MT3-13467-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-MT3-13467-AQ |
467nm |
418nm |
|
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