Gene-specific Copy Number Variation Probe-MPZ
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Catalog: |
CNVFP-MPZ-13240 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MPZ). 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: |
MPZ Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MPZ genes. This product achieves the purpose of detection by hybridizing with the MPZ 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 |
Myelin Protein Zero |
Gene Summary [Provided by RefSeq] |
This gene is specifically expressed in Schwann cells of the peripheral nervous system and encodes a type I transmembrane glycoprotein that is a major structural protein of the peripheral myelin sheath. The encoded protein contains a large hydrophobic extracellular domain and a smaller basic intracellular domain, which are essential for the formation and stabilization of the multilamellar structure of the compact myelin. Mutations in this gene are associated with autosomal dominant form of Charcot-Marie-Tooth disease type 1 (CMT1B) and other polyneuropathies, such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN). A recent study showed that two isoforms are produced from the same mRNA by use of alternative in-frame translation termination codons via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2015] |
Gene Symbol |
MPZ |
Location |
1q23.3 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 161274524-161279762 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-MPZ-13240-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-MPZ-13240-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-MPZ-13240-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-MPZ-13240-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-MPZ-13240-AQ |
467nm |
418nm |
|
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