Gene-specific Copy Number Variation Probe-MTCH2
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Catalog: |
CNVFP-MTCH2-13458 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MTCH2). 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: |
MTCH2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MTCH2 genes. This product achieves the purpose of detection by hybridizing with the MTCH2 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 |
Mitochondrial Carrier 2 |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the SLC25 family of nuclear-encoded transporters that are localized in the inner mitochondrial membrane. Members of this superfamily are involved in many metabolic pathways and cell functions. Genome-wide association studies in human have identified single-nucleotide polymorphisms in several loci associated with obesity. This gene is one such locus, which is highly expressed in white adipose tissue and adipocytes, and thought to play a regulatory role in adipocyte differentiation and biology. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study showed this gene to be an authentic stop codon readthrough target that can produce two isoforms from the same mRNA by use of alternative in-frame translation termination codons. [provided by RefSeq, Dec 2017] |
Gene Symbol |
MTCH2 |
Location |
11p11.2 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 47638857-47664206 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-MTCH2-13458-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-MTCH2-13458-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-MTCH2-13458-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-MTCH2-13458-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-MTCH2-13458-AQ |
467nm |
418nm |
|
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