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Gene-specific Copy Number Variation Probe-TIMM13

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Catalog: CNVFP-TIMM13-20902
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TIMM13). 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: TIMM13 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TIMM13 genes. This product achieves the purpose of detection by hybridizing with the TIMM13 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 Translocase Of Inner Mitochondrial Membrane 13
Gene Summary [Provided by RefSeq] This gene encodes a member of the evolutionarily conserved TIMM (translocase of inner mitochondrial membrane) family of proteins that function as chaperones in the import of proteins from the cytoplasm into the mitochondrial inner membrane. Proteins of this family play a role in collecting substrate proteins from the translocase of the outer mitochondrial membrane (TOM) complex and delivering them to either the sorting and assembly machinery in the outer mitochondrial membrane (SAM) complex or the TIMM22 complex in the inner mitochondrial membrane. The encoded protein and the translocase of mitochondrial inner membrane 8a protein form a 70 kDa complex in the intermembrane space. [provided by RefSeq, Jul 2013]
Gene Symbol TIMM13
Location 19p13.3
Chromosome Chromosome19
Coordinates This gene maps to 2425621-2427875 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-TIMM13-20902-OR 573nm 548nm
2 RE CNVFP-TIMM13-20902-RE 599nm 580nm
3 GO CNVFP-TIMM13-20902-GO 551nm 525nm
4 GR CNVFP-TIMM13-20902-GR 515nm 491nm
5 AQ CNVFP-TIMM13-20902-AQ 467nm 418nm

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