The largest database of trusted experimental protocols

Mitochondria targeted dsred

Manufactured by Takara Bio
Sourced in United States

The Mitochondria targeted DsRed is a fluorescent protein that specifically localizes to the mitochondria within cells. It is derived from the Discosoma sp. red fluorescent protein (DsRed) and is engineered with a mitochondrial targeting sequence to ensure its localization to the mitochondrial compartment.

Automatically generated - may contain errors

2 protocols using mitochondria targeted dsred

1

Lentiviral Production of Mitochondria-Targeted DsRed

Check if the same lab product or an alternative is used in the 5 most similar protocols
Mitochondria targeted DsRed (Clontech) was inserted into lentivirus vector with human polyubiquitin promoter-C (Addgene). HEK293T cells (ATCC, CRL-3216; RRID: CVCL_0063) were transiently cotransfected with lentivirus vector carrying Mitochondria targeted DsRed, packaging vector psPAX2 (Addgene) and envelope vector pMD2.G (Addgene) by using standard calcium phosphate precipitation method. At 24 hr post transfection, the medium was replaced with fresh medium, and lentivirus-containing medium was harvested 24hr later. The virus supernatant was filtered using a 0.45 μm filter (Millipore) to remove cell debris, concentrated by ultracentrifugation (82,700g at 4°C for 2 h), resuspended in neuron culture medium, and stored at −80°C until use.
+ Open protocol
+ Expand
2

Generation of Mitochondria-Targeted Lentivirus

Check if the same lab product or an alternative is used in the 5 most similar protocols
Mitochondria targeted DsRed (Clontech, Mountain View, CA, USA) was inserted into lentivirus vector with human polyubiquitin promoter-C (Addgene, Cambridge, MA, USA). HEK293T cells (ATCC, CRL-3216; RRID: CVCL_0063) were cultured in cell culture medium (DMEM + 10% FBS), one day before transfection, HEK293T cells were sub-cultured into 10 cm dish (Corning) at a density of 6 × 106 cells, after 16 h, the cells were transiently co-transfected with packaging vector psPAX2 (Addgene) and envelope vector pMD2.G (Addgene) by using the standard calcium phosphate precipitation method14 (link). At 24 h post-transfection, the medium was replaced with fresh DMEM and lentivirus-containing medium was harvested 24 h later. The virus supernatant was then filtered using a 0.45 μm PVDF filter (Millipore) to remove cell debris, concentrated by ultracentrifugation (25,000 rpm at 4 °C for 2 h), resuspended in neuron culture medium and stored at − 80 °C until use.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!